Gene Therapy Protocols

Gene Therapy Protocols METHODS IN MOLECULAR MEDICINE TM John M. Walker, SERIES EDITOR 69. Gene Therapy Protocols, 2...

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Gene Therapy Protocols

METHODS IN MOLECULAR MEDICINE

TM

John M. Walker, SERIES EDITOR 69. Gene Therapy Protocols, 2nd ed., edited by Jeffrey R. Morgan, 2002. 68. Molecular Analysis of Cancer, edited by Jacqueline Boultwood and Carrie Fidler, 2002 67. Meningococcal Disease: Methods and Protocols, edited by Andrew J. Pollard and Martin C. J. Maiden, 2001 66. Meningococcal Vaccines: Methods and Protocols, edited by Andrew J. Pollard and Martin C. J. Maiden, 2001 65. Nonviral Vectors for Gene Therapy: Methods and Protocols, edited by Mark A, Findeis, 2001 64. Dendritic Cell Protocols, edited by Stephen P. Robinson and Andrew J. Stagg, 2001 63. Hematopoietic Stem Cell Protocols, edited by Christopher A. Klug and Craig T. Jordan, 2001 62. Parkinson’s Disease: Methods and Protocols, edited by M. Maral Mouradian, 2001 61. Melanoma Techniques and Protocols: Molecular Diagnosis, treatment, and Monitoring, edited by Brian J. Nickoloff, 2001 60. Interleukin Protocols, edited by Luke A. J. O’Neill and Andrew Bowie, 2001 59. Molecular Pathology of the Prions, edited by Harry F. Baker, 2001 58. Metastasis Research Protocols: Volume 2, Cell Behavior In Vitro and In Vivo, edited by Susan A. Brooks and Udo Schumacher, 2001 57. Metastasis Research Protocols: Volume 1, Analysis of Cells and Tissues, edited by Susan A. Brooks and Udo Schumacher, 2001 56. Human Airway Inflammation: Sampling Techniques and Analytical Protocols, edited by Duncan F. Rogers and Louise E. Donnelly, 2001 55. Hematologic Malignancies: Methods and Protocols, edited by Guy B. Faguet, 2001 54. Mycobacterium tuberculosis Protocols, edited by Tanya Parish and Neil G. Stoker, 2001 53. Renal Cancer: Methods and Protocols, edited by Jack H. Mydlo, 2001 52. Atherosclerosis: Experimental Methods and Protocols, edited by Angela F. Drew, 2001

51. Angiotensin Protocols, edited by Donna H. Wang, 2001 50. Colorectal Cancer: Methods and Protocols, edited by Steven M. Powell, 2001 49. Molecular Pathology Protocols, edited by Anthony A. Killeen, 2001 48. Antibiotic Resistance Methods and Protocols, edited by Stephen H. Gillespie, 2001 47. Vision Research Protocols, edited by P. Elizabeth Rakoczy, 2001 46. Angiogenesis Protocols, edited by J. Clifford Murray, 2001 45. Hepatocellular Carcinoma: Methods and Protocols, edited by Nagy A. Habib, 2000 44. Asthma: Mechanisms and Protocols, edited by K. Fan Chung and Ian Adcock, 2001 43. Muscular Dystrophy: Methods and Protocols, edited by Katherine B. Bushby and Louise Anderson, 2001 42. Vaccine Adjuvants: Preparation Methods and Research Protocols, edited by Derek T. O’Hagan, 2000 41. Celiac Disease: Methods and Protocols, edited by Michael N. Marsh, 2000 40. Diagnostic and Therapeutic Antibodies, edited by Andrew J. T. George and Catherine E. Urch, 2000 39. Ovarian Cancer: Methods and Protocols, edited by John M. S. Bartlett, 2000 38. Aging Methods and Protocols, edited by Yvonne A. Barnett and Christopher R. Barnett, 2000 37. Electrochemotherapy, Electrogenetherapy, and Transdermal Drug Delivery: Electrically Mediated Delivery of Molecules to Cells, edited by Mark J. Jaroszeski, Richard Heller, and Richard Gilbert, 2000 36. Septic Shock Methods and Protocols, edited by Thomas J. Evans, 2000 35. Gene Therapy of Cancer: Methods and Protocols, edited by Wolfgang Walther and Ulrike Stein, 2000

METHODS IN MOLECULAR MEDICINE

Gene Therapy Protocols 2nd Edition Edited by

Jeffrey R. Morgan Brown University, Providence, RI

Humana Press

Totowa, New Jersey

TM

© 2002 Humana Press Inc. 999 Riverview Drive, Suite 208 Totowa, New Jersey 07512 www.humanapress.com

All rights reserved. No part of this book may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, microfilming, recording, or otherwise without written permission from the Publisher. The content and opinions expressed in this book are the sole work of the authors and editors, who have warranted due diligence in the creation and issuance of their work. The publisher, editors, and authors are not responsible for errors or omissions or for any consequences arising from the information or opinions presented in this book and make no warranty, express or implied, with respect to its contents. Due diligence has been taken by the publishers, editors, and authors of this book to assure the accuracy of the information published and to describe generally accepted practices. The contributors herein have carefully checked to ensure that the drug selections and dosages set forth in this text are accurate and in accord with the standards accepted at the time of publication. Notwithstanding, since new research, changes in government regulations, and knowledge from clinical experience relating to drug therapy and drug reactions constantly occur, the reader is advised to check the product information provided by the manufacturer of each drug for any change in dosages or for additional warnings and contraindications. This is of utmost importance when the recommended drug herein is a new or infrequently used drug. It is the responsibility of the treating physician to determine dosages and treatment strategies for individual patients. Further, it is the responsibility of the health care provider to ascertain the Food and Drug Administration status of each drug or device used in their clinical practice. The publishers, editors, and authors are not responsible for errors or omissions or for any consequences from the application of the information presented in this book and make no warranty, express or implied, with respect to the contents in this publication. This publication is printed on acid-free paper. ' ANSI Z39.48-1984 (American National Standards Institute) Permanence of Paper for Printed Library Materials. Cover design by Patricia F. Cleary. For additional copies, pricing for bulk purchases, and/or information about other Humana titles, contact Humana at the above address or at any of the following numbers: Tel: 973-256-1699; Fax: 973-256-8341; E-mail: [email protected] or visit our website at http://humanapress.com Photocopy Authorization Policy: Authorization to photocopy items for internal or personal use, or the internal or personal use of specific clients, is granted by Humana Press Inc., provided that the base fee of US $10.00 per copy, plus US $00.25 per page, is paid directly to the Copyright Clearance Center at 222 Rosewood Drive, Danvers, MA 01923. For those organizations that have been granted a photocopy license from the CCC, a separate system of payment has been arranged and is acceptable to Humana Press Inc. The fee code for users of the Transactional Reporting Service is: [0-89603-723-1/02 $10.00 + $00.25]. Printed in the United States of America. 10 9 8 7 6 5 4 3 2 1 Library of Congress Cataloging-in-Publication Data Gene therapy protocols. -- 2nd ed. / edited by Jeffrey R. Morgan. p. ; cm. -- (Methods in molecular medicine ; 69) Includes bibliographical references and index. ISBN 0-89603-723-1 (hardcover; alk. paper) ISBN 0-89603-869-6 (comb binding, alk. paper) 1. Gene therapy--Methodology. I. Morgan, Jeffrey Robert. II. Series. [DNLM: 1. Gene Therapy--methods. 2. Gene Transfer Techniques. 3. Genetic Vectors. QZ 50 G3213 2002] RB155.8 .G465 2002 616'.042--dc21 2001026441

Preface

Efforts in gene therapy have grown dramatically in recent years. Basic research as well as clinical activity have made exciting progress and are beginning to offer renewed hope that gene therapy may be able to deliver novel approaches for the treatment of inherited as well as such acquired diseases as cardiovascular disease and cancer. With the sequencing of the human genome complete, we now have a comprehensive catalog of genes that further expands the potential role of gene therapy into such new fields as tissue engineering. Central to gene therapy is the process of gene transfer; thus, advances in the technology of gene transfer are at the heart of this field’s progress. Numerous technologies, based on a variety of methods (e.g., viral-mediated, physical/ chemical), have been developed to achieve gene transfer. Some of the earliest methods, such as recombinant retroviruses, are still widely used, have undergone significant improvements, and have given rise to new vectors based on lentiviruses. Others, such as molecular conjugates, are exciting new methods that blur the distinctions between the fields of gene therapy and drug delivery. Regardless of the method chosen, gene therapy is performed in either one of two settings, namely ex vivo or in vivo. Individual gene transfer methods have inherent advantages and limitations in these settings and this is an important consideration in planning an overall strategy. Another, perhaps more important, distinction between gene transfer technologies is whether or not the genetic modification is permanent or temporary and this has a large impact on any new medical therapy envisioned. Each of these criteria plays a significant role as the field tries to weigh the advantages and disadvantages of each gene transfer technology and find a match with an intended medical application. The field of gene therapy is advancing simultaneously on several fronts. The core technologies of gene transfer have undergone significant improvements in critical areas such as gene transfer efficiency, gene regulation, and vector production. Industry has joined academia, and a new emphasis is being placed on a quantitative understanding of gene transfer. And the applications of gene transfer continue to expand into new medical areas. In this new and entirely revised second edition, Gene Therapy Protocols presents detailed methods and protocols covering a comprehensive range of technologies and techniques used

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by leaders of the gene therapy field. The first part of the book covers the new molecular conjugates that show great promise for targeting gene transfer and regulating transgene expression. The second part of the book presents completely revised methods based on retroviruses and adenoviruses as well as new and promising methods based on lentiviruses and adeno-associated viruses. The third part of the book details protocols used in exciting applications of gene transfer in such areas as delivery of therapeutic proteins, vaccination, and tissue engineering. This collection of protocols should make a valuable and indispensable resource for graduate students, postdoctoral fellows, as well as basic and clinical researchers in industry and academia. Jeffrey R. Morgan

Contents

Preface ............................................................................................................. v Contributors ..................................................................................................... xi 1 Poly-L-Lysine-Based Gene Delivery Systems: Synthesis, Purification, and Application Charles P. Lollo, Mariusz G. Banaszczyk, Patricia M. Mullen, Christopher C. Coffin, Dongpei Wu, Alison T. Carlo, Donna L. Bassett, Erin K. Gouveia, and Dennis J. Carlo ............. 1 2 Targeted Gene Transfer to Liver Using Protein-DNA Complexes Catherine H. Wu, Cherie M. Walton, and George Y. Wu ................. 15 3 Receptor-Directed Molecular Conjugates for Gene Transfer Assem G. Ziady and Pamela B. Davis ............................................... 25 4 Gene Transfer into Muscle by Electroporation in Vivo Jun-ichi Miyazaki and Hiroyuki Aihara ............................................. 49 5 Viral Liposomes: Preparation and Use Yasufumi Kaneda ................................................................................. 63 6 LPD Nanoparticles—Novel Nonviral Vector for Efficient Gene Delivery Yadi Tan, Mark Whitmore, Song Li, Peter Frederik, and Leaf Huang ................................................................................ 73 7 Solvoplex Synthetic Vector for Intrapulmonary Gene Delivery: Preparation and Use Klaus Schughart and Ulla B. Rasmussen ........................................ 83 8 Gene Correction Frequency by Chimeric RNA-DNA Oligonucleotide Using Nuclear Extracts Olga A. Igoucheva and Kyonggeun Yoon ........................................ 95 9 Regulated Expression of Plasmid-Based Gene Therapies Ronald V. Abruzzese, Fiona C. MacLaughlin, Louis C. Smith, and Jeffrey L. Nordstrom ............................................................. 109 10 Photochemical Transfection: Light-Induced, Site-Directed Gene Delivery Lina Prasmickaite, Anders Høgset, and Kristian Berg ................. 123

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11 Direct Gene Transfer and Vaccination Via Skin Transfection Using a Gene Gun Chia-Feng Kuo, Jeng Hwan Wang, and Ning-Sun Yang ............... 137 12 Preparation of Pseudotyped Retroviral Vector Hong Yu .............................................................................................. 149 13 Quantitative Measurement of the Concentration of Active Recombinant Retrovirus Stelios T. Andreadis and Jeffrey R. Morgan .................................. 161 14 Minigene-Containing Retroviral Vectors Using an Alphavirus/Retrovirus Hybrid Vector System: Production and Use Jarmo Wahlfors and Richard A. Morgan ........................................ 173 15 Retrovirus-Mediated Gene Transfer to Human Hematopoietic Stem Cells William P. Swaney, Enrico M. Novelli, Alfred B. Bahnson, and John A. Barranger ................................................................. 187 16 Genetically Modified Skin Substitutes: Preparation and Use Karen E. Hamoen, Gulsun Erdag, Jennifer L. Cusick, Hinne A. Rakhorst, and Jeffrey R. Morgan ................................ 203 17 Bioartificial Muscles in Gene Therapy Courtney Powell, Janet Shansky, Michael Del Tatto, and Herman H. Vandenburgh ...................................................... 219 18 Cytokine Gene-Modified Cell-Based Cancer Vaccines R. Todd Reilly, Jean-Pascal H. Machiels, Leisha A. Emens, and Elizabeth M. Jaffee ................................................................. 233 19 HIV-Based Vectors: Preparation and Use Antonia Follenzi and Luigi Naldini .................................................. 259 20 Packaging Cell System for Lentivirus Vectors: Preparation and Use Narasimhachar Srinivasakumar ...................................................... 275 21 Lentiviral Vectors: Preparation and Use Lung-Ji Chang and Anne-Kathrin Zaiss ......................................... 303 22 Simian Foamy Virus Vectors: Preparation and Use Jeonghae Park and Ayalew Mergia ................................................. 319 23 Recombinant Feline Immunodeficiency Virus Vectors: Preparation and Use Michael A. Curran and Garry P. Nolan ............................................ 335 24 Lentivirus Vector Based on Simian Immunodeficiency Virus: Development and Use Klaus Überla ....................................................................................... 351

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25 Cytoplasmic RNA Vector Derived from Nontransmissible Sendai Virus: Production and Use Akihiro Iida and Mamoru Hasegawa ............................................... 361 26 Preparation of Helper-Dependent Adenoviral Vectors Philip Ng, Robin J. Parks, and Frank L. Graham ........................... 371 27 Construction of First-Generation Adenoviral Vectors Philip Ng and Frank L. Graham ........................................................ 389 28 Preparation of Ovine Adenovirus Vectors Peter Löser, Daniel Kümin, Moritz Hillgenberg, Gerald W. Both, and Christian Hofmann ................................................................. 415 29 Highly Purified Recombinant Adeno-Associated Virus Vectors: Preparation and Quantitation Bruce Schnepp and K. Reed Clark .................................................. 427 30 High-Titer Stocks of Adeno-Associated Virus from Replicating Amplicons and Herpes Vectors Ajay R. Mistry, Mahesh De Alwis, Elisabeth Feudner, Robin R. Ali, and Adrian J. Thrasher .......................................... 445 31 Herpes Simplex Virus/Adeno-Associated Virus Hybrid Vectors for Gene Transfer to Neurons: Preparation and Use Lauren C. Costantini, Cornel Fraefel, Xandra O. Breakefield, and Ole Isacson ............................................................................. 461 32 Development of Replication-Defective Herpes Simplex Virus Vectors William F. Goins, David M. Krisky, Darren P. Wolfe, David J. Fink, and Joseph C. Glorioso ....................................... 481 Index ............................................................................................................ 509

Contributors

RONALD V. ABRUZZESE • Valentis, The Woodlands, TX HIROYUKI AIHARA • Department of Nutrition and Physiological Chemistry, Osaka University Medical School, Suita, Osaka, Japan ROBIN R. ALI • Molecular Immunology Unit, Institute of Child Health, London; Institute of Ophthalmology, London, United Kingdom STELIOS T. ANDREADIS • Bioengineering Laboratory, Department of Chemical Engineering, University of New York at Buffalo, Amherst, NY ALFRED B. BAHNSON • Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA MARIUSZ G. BANASZCZYK • The Immune Response Corporation, Carlsbad, CA JOHN A. BARRANGER • Department of Human Genetics and Department of Molecular Genetics and Biochemistry, University of Pittsburgh, Pittsburgh, PA DONNA L. BASSETT • The Immune Response Corporation, Carlsbad, CA KRISTIAN BERG • Department of Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway GERALD W. BOTH • CSIRO, North Ryde, Australia XANDRA O. BREAKEFIELD • Molecular Neurogenetics Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA ALISON T. CARLO • The Immune Response Corporation, Carlsbad, CA DENNIS J. CARLO • The Immune Response Corporation, Carlsbad, CA LUNG-JI C HANG • Powell Gene Therapy Center, Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL K. REED CLARK • Division of Molecular Medicine, Department of Pediatrics; Department of Molecular Virology, Immunology, and Molecular Genetics, Ohio State University, Columbus, OH CHRISTOPHER C. COFFIN • The Immune Response Corporation, Carlsbad, CA LAUREN C. COSTANTINI • Neuroregeneration Laboratory, Harvard Medical School; McLean Hospital, Belmont, MA MICHAEL A. CURRAN • Program in Immunology, Stanford University, Stanford, CA

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JENNIFER L. CUSICK • Massachusetts General Hospital, Harvard Medical School; Shriners Hospital for Children, Boston, MA PAMELA B. DAVIS • Department of Pediatrics at Rainbow Babies and Children’s Hospital, Case Western Reserve University, School of Medicine, Cleveland, OH MAHESH DE ALWIS • Molecular Immunology Unit, Institute of Child Health, London; Institute of Ophthalmology, London, United Kingdom MICHAEL DEL TATTO • Department of Pathology, The Miriam Hospital, Cell Based Delivery, Inc., Providence, RI LEISHA A. EMENS • Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD GULSUN ERDAG • Massachusetts General Hospital, Harvard Medical School; Shriners Hospital for Children, Boston, MA ELISABETH FEUDNER • Molecular Immunology Unit, Institute of Child Health, London; Institute of Ophthalmology, London; University Eye Hospital, Tuebingen, Germany DAVID J. FINK • Department of Molecular Genetics and Biochemistry, University of Pittsburgh, School of Medicine, Pittsburgh, PA ANTONIA FOLLENZI • Laboratory for Gene Transfer and Therapy IRCC, Institute for Cancer Research and Treatment, University of Torino Medical School, Torino, Italy CORNEL FRAEFEL • University Institute for Virology, Zurich, Switzerland PETER FREDERIK • Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA JOSEPH C. GLORIOSO • Department of Molecular Genetics and Biochemistry, University of Pittsburgh, School of Medicine, Pittsburgh, PA WILLIAM F. GOINS • Department of Molecular Genetics and Biochemistry, University of Pittsburgh, School of Medicine, Pittsburgh, PA ERIN K. GOUVEIA • The Immune Response Corporation, Carlsbad, CA FRANK L. GRAHAM • Departments of Biology and Pathology, McMaster University, Hamilton, Ontario, Canada KAREN E. HAMOEN • Massachusetts General Hospital, Harvard Medical School; Shriners Hospital for Children, Boston, MA MAMORU HASEGAWA • DNAVEC Research Inc., Tsukuba-shi, Japan MORITZ HILLGENBERG • DeveloGen AG, NL Berlin, Berlin-Buch, Germany CHRISTIAN HOFMANN • DeveloGen AG, NL Berlin, Berlin-Buch, Germany ANDERS HØGSET • Department of Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway

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LEAF HUANG • Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA OLGA A. IGOUCHEVA • Department of Dermatology and Cutaneous Biology, Department of Biochemistry and Molecular Pharmacology, Jefferson Institute of Molecular Medicine, Jefferson Medical College, Philadelphia, PA AKIHIRO IIDA • DNAVEC Research Inc., Tsukuba-shi, Ibaraki, Japan OLE ISACSON • Neuroregeneration Laboratory, Harvard Medical School; McLean Hospital, Belmont, MA ELIZABETH M. JAFFEE • Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD YASUFUMI KANEDA • Division of Gene Therapy Science, Graduate School of Medicine, Osaka, University, Suita Osaka, Japan DAVID M. KRISKY • Department of Molecular Genetics and Biochemistry, University of Pittsburgh, School of Medicine, Pittsburgh, PA DANIEL KÜMIN • DeveloGen AG, NL Berlin, Berlin-Buch, Germany CHIA-FENG KUO • Department of Foods & Nutrition, Shih-Chen University, Institute of Bioagricultural Science, Academia Sinica, Taipei, Taiwan SONG LI • Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA CHARLES P. LOLLO • Target Protein Technologies, San Diego, CA PETER LÖSER • DeveloGen AG, NL Berlin, Berlin-Buch, Germany JEAN-PASCAL H. MACHIELS • Laboratoire d'Oncologie Experimentale, Université Catholique de Louvain, Russels, Belgium FIONA C. MACLAUGHLIN • Valentis, The Woodlands, TX AYALEW MERGIA • Department of Pathobiology, College of Veterinary Medicine, University of Florida, Gainsville, FL AJAY R. MISTRY • Molecular Immunology Unit, Institute of Child Health, London; Institute of Ophthalmology, London, United Kingdom JUN-ICHI MIYAZAKI • Department of Nutrition and Physiological Chemistry, Osaka University Medical School, Suita, Osaka, Japan JEFFREY R. MORGAN • Brown University, Providence, RI; Massachusetts General Hospital, Harvard Medical School and Shriners Hospital for Children, Boston, MA RICHARD A. M ORGAN • Clinical Gene Therapy Branch, National Human Genome Research Institute, National Institute of Health, Bethesda, MD PATRICIA M. MULLEN • The Immune Response Corporation, Carlsbad, CA

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LUIGI NALDINI • Laboratory for Gene Transfer and Therapy IRCC, Institute for Cancer Research and Treatment, University of Torino Medical School, Torino, Italy PHILIP NG • Departments of Biology and Pathology, McMaster University, Hamilton, Ontario, Canada GARRY P. NOLAN • Department of Molecular Pharmacology, Stanford University, Stanford, CA JEFFREY L. NORDSTROM • Valentis, The Woodlands, TX ENRICO M. NOVELLI • Department of Human Genetics and Department of Molecular Genetics and Biochemistry, University of Pittsburgh, Pittsburgh, PA JEONGHAE PARK • Department of Pathobiology, College of Veterinary Medicine, University of Florida, Gainsville, FL ROBIN J. PARKS • Ottawa Health Research Institute, Ottawa, Ontario, Canada COURTNEY POWELL • Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University; Department of Pathology, The Miriam Hospital, Providence, RI LINA PRASMICKAITE • Department of Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway HINNE A. RAKHORST • Massachusetts General Hospital, Harvard Medical School Shriners Hospital for Children, Boston, MA ULLA B. RASMUSSEN • Laboratory of Molecular and Cellular Biology, TRANSGENE S.A., Strasbourg, France R. TODD REILLY • Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD BRUCE SCHNEPP • Children’s Research Institute, Children’s Hospital Inc., Columbus, OH KLAUS SCHUGHART • Laboratory of Molecular and Cellular Biology, TRANSGENE S.A., Strasbourg, France JANET SHANSKY • Cell Based Delivery, Inc., Providence, RI LOUIS C. SMITH • Valentis, The Woodlands, TX NARASIMHACHAR SRINIVASAKUMAR • Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN WILLIAM P. SWANEY • Department of Molecular Genetics and Biochemistry, University of Pittsburgh, Pittsburgh, PA YADI TAN • Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA

Contributors

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ADRIAN J. THRASHER • Molecular Immunology Unit, Institute of Child Health, London; Institute of Ophthalmology, London, United Kingdom KLAUS ÜBERLA • Department of Molecular and Medical Virology, Ruhr University Bochum, Bochum, Germany HERMAN H. VANDENBURGH • Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University; Cell Based Delivery, Department of Pathology, The Miriam Hospital, Providence, RI JARMO WAHLFORS • A.I. Virtanen Institute for Molecular Sciences, University of Kuopio, Kuopio, Finland CHERIE M. WALTON • Division of Gastroenterology-Hepatology, Department of Medicine, University of Connecticut Health Center, Farmington, CT JENG HWAN WANG • Department of Foods & Nutrition, Shih-Chen University, Institute of Bioagricultural Science, Academia Sinica, Taipei, Taiwan MARK WHITMORE • Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA DARREN P. WOLFE • Department of Molecular Genetics and Biochemistry, University of Pittsburgh, School of Medicine, Pittsburgh, PA CATHERINE H. WU • Division of Gastroenterology-Hepatology, Department of Medicine, University of Connecticut Health Center, Farmington, CT DONGPEI WU • The Immune Response Corporation, Carlsbad, CA GEORGE Y. WU • Division of Gastroenterology-Hepatology, Department of Medicine, University of Connecticut Health Center, Farmington, CT NING-SUN YANG • Department of Foods & Nutrition, Shih-Chen University, Institute of Bioagricultural Science, Academia Sinica, Taipei, Taiwan KYONGGEUN YOON • Department of Dermatology and Cutaneous Biology, Department of Biochemistry and Molecular Pharmacology, Jefferson Institute of Molecular Medicine, Jefferson Medical College, Philadelphia, PA HONG YU • Department of Surgery/Vascular Division, Keck School of Medicine, University of Southern California, Los Angeles, CA ANNE-KATHRIN ZAISS • Powell Gene Therapy Center, Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL ASSEM G. ZIADY • Department of Pediatrics at Rainbow Babies and Children's Hospital, Case Western Reserve University, School of Medicine, Cleveland, OH

Poly-L-Lysine-Based Gene Delivery Systems

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1 Poly-L-Lysine-Based Gene Delivery Systems Synthesis, Purification, and Application Charles P. Lollo, Mariusz G. Banaszczyk, Patricia M. Mullen, Christopher C. Coffin, Dongpei Wu, Alison T. Carlo, Donna L. Bassett, Erin K. Gouveia, and Dennis J. Carlo

1. Introduction Nonviral gene delivery has great potential for replacement of recombinant protein therapy. In many cases, gene therapies would be a considerable improvement over existing therapies because of putative advantages in dosing schedule, patient compliance, toxicity, immunogenicity, and cost. Development of a nonviral gene delivery vehicle capable of efficient, cell-specific delivery will be a valuable addition to the clinical armamentarium. The current situation has led to a focus on increasingly complex delivery systems as investigators try to achieve the delivery efficiency that viral systems already demonstrate. It will be very difficult to create a self-assembling gene delivery system that incorporates molecular mechanisms similar to those that allow viruses to trespass on vascular, cellular, and intracellular barriers and effectively deliver viral DNA to the nucleus of mammalian cells. However, much progress has been made with regard to production of uniform particles. Steric stabilization of materials in vascular compartments has been an area of intense investigation, and numerous strategies for surface modification of delivery vehicles have shown positive effects (1–6). Incorporation of molecular components to accomplish receptor-mediated targeting, endosomal escape, and nuclear transport have all been attempted, with some success in vitro (7,8). From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Sample grafts.

1.1. Poly-L-Lysine Poly-L-lysine (PLL) is a linear, biodegradable polymer that can be readily modified with a variety of chemical reagents to create novel conjugates with enhanced characteristics over those present in PLL per se. In the gene delivery arena, researchers have typically tried to mimic characteristics of proteins that enable viruses to deliver their DNA or RNA payload so efficiently. Thus, many synthetic chemists have focused on incorporating moieties that can facilitate cell-specific targeting, membrane penetration, and nuclear transport. Another common synthetic goal is to modify PLL so that it can protect the DNA payload effectively. More specifically, the intent is to diminish deleterious in vivo interactions such as immunogenicity, toxicity, adventitious binding, and uptake by the reticuloendothelial system. PLL can be grafted with various agents to alter polyplex performance characteristics depending on desired outcome and area of investigation. Cationic polymers other than PLL have also been modified and characterized in a similar fashion (9–11).

1.2. Grafting Grafts can consist of any natural or synthetic polymer, linear or branched, cyclic, heterocyclic, containing heteroatoms, or any combination of grafting molecules. The number of grafted chains can be varied to suit specific applications (Fig. 1).


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Fig. 2. Grafting of receptor ligands onto a cationic polymer.

Fig. 3. Reaction of an activated ester with an amino group. An amide bond-linked conjugate is produced.

1.3. Ligand To achieve cell-specific targeting, receptor ligands can be grafted onto PLL or other cationic polymers (12–14). The preferred position of a ligand is on the exterior surface to ensure proper ligand recognition. However, it is conceivable that ligands may also be partially buried and subject to molecular mechanisms that expose them at an appropriate time (15). Polymers, like polyethylene glycol (PEG), that are grafted onto surfaces form statistical clouds that are continually in flux. Therefore, simple covalent attachment of ligand onto the terminal end of a polymeric chain does not guarantee ligand recognition. The linker polymer, graft density, and chemistry will probably have to be optimized for individual cases (Fig. 2).

1.4. Graft Attachment Nucleophilic substitution of activated esters is the most common chemistry to graft polymeric chains onto amino groups of proteins, cationic polymers, or more specifically PLL (16). The reaction of an activated ester with an amino group produces an amide bond-linked conjugate and results in a net loss of charge on the conjugate (Fig. 3). This loss of positive charge along the polymer chain significantly weakens the binding of conjugate to DNA. Conversely, chemistry that preserves the charge of the cationic domain is expected to have a lessened impact on DNA

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Fig. 4. Reaction of an electrophilic reagent with an ε-amino group of PLL.

binding since the binding will be affected only by steric hindrance generated from the grafted moieties. For synthesis of our conjugates, we have chosen chemistries that preserve charges on the cationic domain and typically produce secondary and tertiary amines, and rarely quaternary ammonium species. All these amine species bear a positive charge at physiologic pH and consequently will bind to DNA electrostatically. The first method described below uses PEG–epoxide as the electrophilic reagent that reacts with ε-amino groups of PLL. The product of the reaction is a secondary amine with a racemic βhydroxyl group (Fig. 4). Grafts can be added successively if more than one feature is desired. Alternatively, the grafting molecule can be engineered to contain more than one functional domain.

1.5. Conjugate Synthesis, Purification, and Characterization A variety of grafted PLL conjugates have been successfully synthesized (17). These copolymers (e.g., poly-L-lysine-graft-R1-graft-R2-graft-R3) can have a variety of molecules grafted on amino groups of cationic polymers in a stepwise synthesis. For example, PEG molecules can be grafted first (R1), followed by introduction of other functional groups such as ligands (R2), and finally fluorescent tags or other delivery-enhancing moieties (R3). The synthesis of one grafted copolymer is described below in stepwise fashion. The procedure can be repeated to add other grafted domains. 2. Materials 2.1. Chemicals 1. 2. 3. 4. 5. 6. 7. 8. 9. 10.

Phosphate (J.T. Baker, Phillipsburg, NJ). SP Sepharose FF resin (Amersham Pharmacia, Uppsala, Sweden). NaOH (J.T. Baker). NaCl (J.T. Baker). PLL 10K (Sigma, St. Louis, MO). Lithium hydroxide monohydrate (E.M. Science, Gibbstown, NJ). Methanol (VWR Scientific Products, West Chester, PA). BioCad 700E HPLC (PE Biosystems, Foster City, CA). UV/VIS detector (PE Biosystems). Glacial acetic acid (J.T. Baker).

Poly-L-Lysine-Based Gene Delivery Systems 11. 12. 13. 14. 15. 16. 17. 18. 19. 20.

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PEG5K-epoxide (Shearwater Polymers, Huntsville, AL). Sephadex G-25 fine resin (Amersham Pharmacia). Trilactosyl aldehyde (Contract synthesis, e.g., SRI International, Menlo Park, CA). Amino-PEG3.4k-amino-tBOC (Shearwater Polymers). Sodium cyanoborohydride (Alfa Aesar, Ward Hill, MA). Methyl iodide (Aldrich, Milwaukee, WI). Trifluoroacetic acid (J.T. Baker). Methylene chloride (VWR Scientific Products). Succinimidyl bromoacetate (Molecular Biosciences, Boulder, CO). Acetonitrile (J.T. Baker).

2.2. Materials for DNA Manipulation 1. Tris(hydroxymethyl)aminomethane (J.T. Baker). 2. EDTA (J.T. Baker). 3. Ethidium bromide (Sigma).

2.3. Materials for Animal Studies 1. 2. 3. 4. 5. 6. 7.

Ketamine (Phoenix Pharmaceuticals, St. Joseph, MO). Xylazine (Phoenix Pharmaceuticals). Acepromazine (Fermenta Vet. Products, Kansas City, MO). Potassium phosphate (J.T. Baker). Triton X-100 (VWR Scientific Products). Sigma Firefly luciferase L-5256 (BD Pharmingen, San Diego, CA). 15-mL dounce homogenizer (Wheaton, Millville, NJ).

3. Methods 3.1. Synthesis of Poly-L-Lysine-graft-R1-graft-R2-graft-R3 Copolymers R1 means PEG derivative and R2 and R3 no PEG derivative. PLL-graft-PEG polymers can be prepared by reaction of a PEG-electrophile with ε-NH2 lysine groups under basic conditions. For any specific copolymers, the ratio of activated PEG to poly-L-lysine, PEG size, and poly-L-lysine size can be varied as needed. 1. Poly-L-lysine 10K (600 mg, 0.06 mmol) and lithium hydroxide monohydrate (41 mg, 2.9 mmol) are dissolved in water (2 mL) and methanol (6 mL) in a siliconized glass flask. 2. Solid PEG5K-epoxide (600 mg, 0.12 mmol) is added to the flask, which is then sealed, and the solution is incubated at 65°C for 48 h. 3. After incubation, the solvent is removed in vacuo. The product is redissolved in a loading buffer (0.1 M sodium phosphate, pH 6, in 10% MeOH [v/v]). 4. The solution is loaded on a cation exchange column (SP Sepharose FF resin) attached to a high-performance liquid chromatography (HPLC) device (e.g., BioCad 700E), followed by an extensive washing step (up to 10 column volumes).

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Lollo et al. 5. The product is eluted with 0.1 N NaOH in 10% MeOH solution. An in-line 214nm UV/VIS detector is used to monitor the eluant, and fractions are collected in a standard manner. 6. Fractions containing the product are combined and neutralized, and the solvent is removed in vacuo. 7. The dried product, which contains inorganic salts, is redissolved in a minimum amount of 0.05 M acetic acid in 30% MeOH solution and separated over a G-25 column (Amersham Pharmacia Sephadex G-25 fine resin) using the same acetic acid solution. 8. The fractions are pooled and lyophilized. The average number of PEG moieties grafted onto each poly-L-lysine chain can be determined by 1H nuclear magnetic resonance (NMR) (18).

3.2. Synthesis of PL26k-graft-(ε-NH-CH2CO-NH-PEG-εTrilactose-Ligand)2.5 Stepwise grafting is one of the simplest ways to modulate properties of resulting copolymers. However, it does not provide easy means of incorporating targeting moieties at their optimal positions. The linker bearing the ligand should be at least as long (or longer) as other components grafted onto the cationic domain. Otherwise, the ligand could be buried and thus unavailable for binding interactions. Several heterobifunctional PEGs (abbreviated as X-PEG-Y) are commercially available in a 3.4-kDa size. These X-PEG-Y molecules can be used to connect ligands to cationic domains. An example of this type of synthesis is shown in Fig. 5. 1. Trilactosyl aldehyde (100 mg, 0.067 mmol) is stirred in water (0.5 mL) under argon. 2. Amino-PEG3.4k-amino-t-BOC (151 mg, 0.04 mmol) and lithium hydroxide (1.7 mg, 0.04 mmol) dissolved in methanol (1 ml) are then added to the trigalactosyl aldehyde solution and stirred under argon at 25°C for 30 min. 3. Two portions of sodium cyanoborohydride (6.2 mg, 0.1 mmol) are then added over a 24-h period. 4. Methyl iodide (568 mg, 4 mmol) is added and the solution stirred for 24 h. 5. The solution is then evaporated to dryness, and trifluoroacetic acid (0.7 mL) in methylene chloride (0.6 mL) is added. 6. The solvents are again evaporated to dryness and the residue redissolved in a mixture of methanol and water (3 mL). 7. The solution is adjusted to pH 9 with 10 N sodium hydroxide. Succinimidyl bromoacetate (118.5 mg, 0.5 mmol) is then added in acetonitrile (0.5 mL), and the mixture is stirred under argon at 25°C for 1 h. 8. The bromoacetyl intermediate is eluted over a Sephadex G-25 column in 0.05 N acetic acid. 9. The macromolecular fractions are combined and evaporated in vacuo. 10. Poly-L-lysine 26k (27.7 mg, 0.001 mmol) and lithium hydroxide (4.6 mg, 0.11

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Fig. 5. An example of stepwise grafting.


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mmol) dissolved in methanol (1.5 mL) are added to the solution of iodoacetyl intermediate. 11. The reaction mixture is sealed and incubated overnight at 37°C. 12. The product is purified by SP Sepharose FF and Sephadex G-25 column chromatography. 13. The ratio of triantennary galactose/PEG/PLL is determined by 1H NMR.

3.3. 1H NMR Spectroscopy 1. Each polymer is first freeze-dried from D2O and redissolved in D2O for spectral analysis. This procedure minimizes the HOD peak and gives superior spectra. 2. 1H NMR spectra are recorded on a high-resolution spectrometer (e.g., 300 MHz ARX-300 Bruker). 3. Chemical shifts are expressed in parts per million and referenced to the HDO signal at 4.7 ppm. 4. The integration ratio of PEG signal (3.68 ppm) to Cα-H of poly-L-lysine (4.2 ppm) is used to determine the composition of the copolymer. 5. The number of Cα-H protons per PLL molecule is calculated from the MW and known structure. For example, 10-kDa polylysine has 48 Cα-H. 6. The number of methylene protons (–CH2-) per PEG molecule is calculated from the MW and known structure. For example, 5-kDa PEG has 454 methylene protons. 7. The number determined in step 6 is divided by the number determined in step 5 to yield the proton ratio expected for a 1:1 conjugation of PEG and PL. 8. The ratio computed in step 4 is divided by the ratio computed in step 7 to yield the average number of PEG grafts per PLL molecule.

3.4. Plasmid DNA Preparation and purification of plasmid DNA is beyond the scope of this chapter, but a few salient points need to be made as to the use of plasmid DNA for polyplex formation and transfection studies. These remarks assume that the plasmid was constructed properly, contains the proper elements, and is known to express at reasonable levels in transfection assays in vitro. Plasmid DNA should be assayed by agarose gel electrophoresis with ethidium bromide staining to determine purity and relative amounts of linear and covalently closed circular forms including the super-coiled form. For best results, plasmid DNA used in transfection studies should be ≥90% in the covalently closed circular form. Plasmid DNA should be stored below 4°C in an appropriate buffer (e.g., 10 mM Tris(hydroxymethyl)aminomethane, 1 mM EDTA, pH 8.0). DNA preparations must be tested for endotoxin levels using the limulus amebocyte lysate assay (Bio-Whittaker, Walkersville, MD) or other methods (19). Contamination should not exceed 10 endotoxin units per milligram of plasmid DNA.


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3.5. Charge Ratio Determinations Charge ratios (+/-) can be determined by several methods, and it is recommended that at least two independent methods be used to characterize conjugates. We recommend using a theoretical calculation based on composition combined with a fluorescence quenching assay.

3.6. Calculation Based on Composition 1. From the proton NMR data, calculate the expected molecular weight of the conjugate. 2. From the known composition of the conjugate, calculate the number of positive charges on each conjugate molecule. 3. Calculate the conjugate mass per positive charge (step 1/step 2). 4. The mean mass per unit negative charge for plasmid DNA is 330. 5. Conjugate mass per unit charge (step 3) divided by DNA mass per unit charge (330) is the theoretical mass ratio (R) to form a neutral polyplex. 6. To manufacture a polyplex at a given charge ratio, use the following equation: mass of conjugate = desired polyplex charge ratio × DNA mass × R

3.7. Fluorescence Quenching Assay The binding abilities of polycationic polymers were examined using an ethidium bromide-based quenching assay. 1. Solutions (1 mL) containing 2.5 μg/mL ethidium bromide and 10 μg/mL DNA (1:5 molar ratio, EtBr/DNA phosphate) are prepared. 2. Highly concentrated aqueous conjugate solutions (≥1 mg/mL) are used to minimize the effect of dilution after multiple additions. 3. Fluorescence reading is taken of the DNA solution prepared in step 1, using a fluorometer with excitation and emission wavelengths at 540 and 585 nm, respectively. 4. Aliquots of the conjugate solution prepared in step 2 are added incrementally to the DNA solution, and fluorescence readings are taken after each addition. Aliquots should be 6 h before harvesting the virus. 6. Partially remove the egg shell and remove the chorioallantoic fluid to an autoclaved bottle using a 10-mL syringe with an 18-gage needle. The virus in the fluid stored at 4°C is stable at least for 3 months.

Steps 2, 3 and 6 can be carried out at room temperature. 3.2. Purification of HVJ from Chorioallantoic Fluid 1. Transfer 200 mL of the chorioallantoic fluid into four 50-mL disposable conical tubes, rotate at 1000g for 10 min at 4°C in a low-speed centrifuge. 2. Then aliquot the supernatant into six tubes (JS-20; Beckman) and centrifuge at 27,000g for 30 min at 4°C. 3. Add about 5 mL of BSS to the pellet in one of the tubes, and keep the materials at 4°C overnight.

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4. Gently suspend the pellets, collect in two tubes, and centrifuge as described in step 2. Keep the resultant pellet in each tube at 4°C in 5 mL of BSS for more than 8 h. 5. Gently suspend the pellets and rotate at 1000g in a low-speed centrifuge. 6. Remove the supernatant to an aseptic tube and store at 4°C. 7. Indicate virus titer by measuring the absorbance at 540 nm of the 10× diluted supernatant using a photometer. An optical density at 540 nm corresponds to 15,000 hemagglutinating units (HAU), which correlates well with fusion activity. The supernatant prepared as above usually shows 20,000–30,000 HAU/mL. An aseptically prepared virus solution maintains the fusion activity for 3 weeks.

3.3. Preparation of Lipid Mixture 1. Dissolve dry reagents of DOPE (12.2 mg), Sph (11.8 mg), and Chol (24.0 mg) in 3870 μL of chloroform. Add 130 μL of PC (13.0 mg) chloroform solution to the 3870-μL lipid solution (see Note 1). This 4000-μL lipid solution is called a basal mixture for liposomes. The basal mixture is ready for preparation of the anionic or cationic liposomes described below, or it can be stored at –20°C after infusing nitrogen gas. 2. To prepare the anionic lipid mixture, add 10 mg of PS to the basal mixture. To obtain the cationic lipid mixture, add 6 mg of DC to the mixture. 3. Aliquot the lipid solution of 0.5 mL into eight glass tubes. Keep the tubes on ice or –20°C in nitrogen gas before evaporation. Evaporate the lipid solution as soon as possible. 4. Connect the tube to a rotary evaporator. Immerse the tube in a water bath at the tip, and set the water bath at a temperature of 40°C. 5. Evaporate the organic solvent in a rotary evaporator in a vacuum. The usual drying period is about 5–10 min. Lipids appropriate for liposome preparation are those that have stuck inside the tube in a thin layer. Those that have accumulated at the bottom of the tubes are inappropriate (see Note 2).

3.4. Preparation of HVJ Liposomes Containing DNA 1. Add plasmid DNA (200 μg) in 200 μL BSS to a lipid mixture in the glass tube prepared as above and agitate intensely by vortexing for 30 s followed by incubation at 37°C for 30 s. Repeat this cycle eight times. By this method, plasmid DNA is enclosed at a ratio of 10–30% in anionic liposomes or 50–60% in cationic liposomes. 2. For preparation of sized unilamellar liposomes, filter the liposome suspension with 0.45-μm pore size cellulose acetate filter and then with 0.2-μm filter. Sizing by an extruder with polycarobanate filters is better for preparing sized liposomes. 3. In the meantime, inactivate the HVJ virus and keep on ice (see Note 3). Add 15,000 HAU of the HVJ virus to the liposome suspension and leave the tube on ice for 5–10 min (see Note 4). Then incubate sample at 37°C for 1 h with shaking (120/min) in a water bath. 4. Add 7 mL 30% sucrose solution to a centrifuge tube and overlay the HVJ lipo-

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some mixture on it. Separate the HVJ-liposome complexes from the free HVJ by sucrose gradient density centrifugation at 62,000g for 90 min at 4°C. 5. Stop the centrifuge and gently remove only the conjugated liposomes. The final volume of the HVJ-liposome suspension should be approximately 1 mL. 6. Only in the case of HVJ-anionic liposomes, after centrifugation, collect the complexes, add 4 vol of chilled BSS, spin at 27,000g for 30 min, and suspend the pellet in 0.5–1.0 mL of appropriate buffer (see Note 5).

3.5. Applications 3.5.1. Transfer of DNA into Cultured Cells 1. HVJ-cationic liposomes should be used for in vitro gene transfer because HVJcationic liposomes are approximately 100 times more efficient in gene transfer to cultured cells than HVJ-anionic liposomes (7). Add 10 μL of 1-mL HVJ-cationic liposome suspension to 105 cells in serum-containing culture medium (14). 2. Incubate the cells with the liposomes at 37°C for 2 h. Then change to fresh medium and continue the culture (see Note 6).

3.5.2. Gene Transfer In Vivo by HVJ Liposomes 1. For gene transfer to tissues, HVJ-anionic liposomes are recommended. The liposomes are useful for gene transfer to liver, skeletal muscle, heart, lung, artery, brain, spleen, eye, and joint space of rodent, rabbit, dog, lamb, and monkey. For example, to introduce DNA into rat liver, inject 2–3 mL of HVJ-anionic liposomes into the portal vein using a 5-mL syringe with a butterfly-shaped needle (15,16) or directly into the liver under the perisplanchnic membrane using a 5mL syringe with a 27-gage needle (17,18). For gene transfer into rat kidney, inject 1 mL of anionic HVJ-liposome suspension into the renal artery (19,20). For gene transfer to rat carotid artery, fill a lumen of a segment of the artery with 0.5 mL anionic HVJ-liposome complex for 20 min at room temperature using a cannula (21). 2. For gene transfer to tumor masses or disseminated tumors, direct injection of cationic HVJ liposomes (0.1–0.5 mL) is recommended.

4. Notes 1. Lipid vials should be left at room temperature for about 30 min before opening the lids. Many lipids are highly hygroscopic. 2. The lipid mixture in the glass tube can be stored at –20°C in nitrogen gas for 1 month, after evaporation. 3. UV-inactivated HVJ can be stored for >6 months in 10% DMSO at –80°C. Do not store it at 4°C for more than 1 day. 4. Reconstituted fusion liposomes can be prepared using isolated fusion proteins derived from HVJ instead of inactivated whole viral particles (23).

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5. HVJ liposomes can be stored for 3 weeks at 4°C and for more than 3 months with 10% DMSO at the final concentration in a freezer (below –20°C). 6. Gene transfer efficiency of HVJ liposomes is greatly affected by the fusion activity of the HVJ envelope. The hemagglutinating ability should be frequently checked by hemagglutination of chick red blood cells (22).

References 1. Mulligan, R. C. (1993) The basic science of gene therapy. Science 260, 926–932. 2. Ledley, F. D. (1995) Non-viral gene therapy: the promise of genes as pharmaceutical products. Hum. Gene Ther. 6, 1129–1144. 3. Kaneda, Y. (1998) Fusigenic Sendai-virus liposomes: a novel hybrid type liposome for gene therapy. Biogenic Amines 14, 553–572. 4. Kaneda, Y., Saeki, Y., Morishita, R. (1999) Gene therapy using HVJ-liposomes; the best of both worlds. Mol. Med. Today 5, 298–303. 5. Dzau, V. J., Mann, M., Morishita, R., and Kaneda, Y. (1996) Fusigenic viral liposome for gene therapy in cardiovascular diseases. Proc. Natl. Acad. Sci. USA 93, 11421–11425. 6. Hirano, T., Fujimoto, J., Ueki, T., et al. (1998) Persistent gene expression in rat liver in vivo by repetitive transfections using HVJ-liposome. Gene Ther. 5, 459–464. 7. Saeki, Y., Matsumoto, N., Nakano, Y., et al. (1997) Development and characterization of cationic liposomes conjugated with HVJ (Sendai virus): reciprocal effect of cationic lipid for in vitro and in vivo gene transfer. Hum. Gene Ther. 8, 1965–1972. 8. Chander, R. and Schreier, H. (1992) Artificial viral envelopes containing recombinant human immunodeficiency virus (HIV) gp160. Life Sci. 50, 481–489. 9. Sawa, Y., Kaneda, Y., Bai, H.-Z., et al. (1998) Efficient transfer of oligonucleotides and plasmid DNA into the whole heart through the coronary artery. Gene Ther. 5, 1472–1480. 10. Goyal, K. and Huang, L. (1995) Gene therapy using DC-Chol liposomes. J. Liposome Res. 5, 49–60. 11. Yamada, G., Nakamura, S., Haraguchi, R., et al. (1997) An efficient liposomemediated gene transfer into the branchial arch, neural tube and the heart of chick embryos: a strategy to elucidate organogenesis. Cell. Mol. Biol. 43, 1165–1169. 12. Yonemitsu, Y., Kaneda, Y., Muraishi, A., et al. (1997) HVJ (Sendai virus)-cationic liposomes: a novel and potentially effective liposome-mediated gene transfer technique to the delivery to the airway epithelium. Gene Ther. 4, 631–638. 13. Mabuchi, E., Shimizu,K., Miyao,Y., et al. (1997) Gene delivery by HVJ-liposome in the experimental gene therapy of murine glioma. Gene Ther. 4, 768–772. 14. Nishikawa, T., Edelstein, D., Du, X.L., et al. (2000) Normalization of mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature 404, 787–790.

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15. Kaneda, Y., Iwai, K., and Uchida,T. (1989) Increased expression of DNA cointroduced with nuclear protein in adult rat liver. Science 243, 375–379. 16. Kaneda, Y., Iwai, K., and Uchida, T. (1989) Introduction and expression of the human insulin gene in adult rat liver. J. Biol. Chem. 264, 12126–12129. 17. Kato, K., Nakanishi, M., Kaneda, Y., Uchida, T., and Okada, Y. (1991) Expression of hepatitis B virus surface antigen in adult rat liver. J. Biol. Chem. 266, 3361–3364. 18. Tomita, N., Morishita, R., Higaki, J., et al. (1996) In vivo gene transfer of insulin gene into neonatal rats by HVJ-liposome method resulted in sustained transgene expression. Gene Ther. 3, 477–482. 19. Tomita, N., Higaki, J. , Morishita, R., et al. (1992) Direct in vivo gene introduction into rat kidney. Biochem. Biophys. Res. Commun. 186, 129–134. 20. Isaka, Y., Fujiwara, Y., Ueda, N., et al. (1993) Glomerulosclerosis induced by in vivo transfection with TGF-β or PDGF gene into rat kidney. J. Clin. Invest. 92, 2597–2601. 21. Morishita, R., Gibbons, G., Kaneda, Y., Ogihara, T., and Dzau, V. (1993) Novel and effective gene transfer technique for study of vascular renin angiotensin system. J. Clin. Invest. 91, 2580–2585. 22. Okada, Y. and Tadokoro, J. (1962) Analysis of giant polynuclear cell formation caused by HVJ virus from Ehrlich‘s ascites tumor cells. Exp. Cell Res. 26, 98– 128. 23. Suzuki K, Nakashima H, Sawa Y, et al. (2000) Reconstituted fusion liposomes for gene transfer in vitro and in vivo. Gene Ther. Reg. 1, 65–77.

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6 LPD Nanoparticles—Novel Nonviral Vector for Efficient Gene Delivery Yadi Tan, Mark Whitmore, Song Li, Peter Frederik, and Leaf Huang

1. Introduction 1.1. Composition Liposome-Polycation-DNA (LPD) nanoparticles is a novel nonviral vector developed in our laboratory for efficient systemic gene delivery. Currently there are two LPD formulations in use, differing in cationic liposome composition. One is composed of cationic lipid dioleoyl-trimethylammonium propane (DOTAP) and cholesterol at molar ratio of 1:1. The other is composed of cationic lipid 3ß(N-(N', N'-dimethylaminoethane) carbamoyl) cholesterol (DCChol) and neutral lipid dioleoylphosphatidylethanolamine (DOPE) at a molar ratio of 6:4. The polycation component is added for the condensation of plasmid DNA. Polylysine first was used (1), and later it was changed to protamine sulfate for improved activity (2). The optimal composition for DOTAP/cholesterol LPD is 1200 nmol DOTAP/1200 nmol cholesterol/60 μg protamine sulfate/100 μg plasmid DNA, which has a charge ratio of 4:1 (+:–) between DOTAP and DNA and a 1/1 charge ratio between protamine and DNA. The optimal composition for DC-Chol/DOPE LPD is 60 nmol total lipids (36 nmol DC-Chol and 24 nmol DOPE)/80 μg protamine/100 μg plasmid DNA. 1.2. Preparation, Physical Property, and Storage The LPD nanoparticles are prepared by adding an equal volume of DNA solution to an aqueous mixture of cationic liposome and protamine sulfate in a dropwise manner. The resulting tertiary complex contains a highly condensed From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Cryoelectron micrograph of LPD. Scale bar = 100 nm.

DNA core surrounded by lipid bilayers (Fig. 1). LPD nanoparticles range from 30–200 nm in diameter, with an average of about 100 nm. It can be stored as solution at 4°C for at least 4 weeks without losing activity. Alternatively, it can be stored for more than a year at room temperature as a lyophilized powder and is fully active after reconstitution (3). 1.3. Biologic Activity When DOTAP/cholesterol LPD containing a marker gene is injected from the tail vein of a mouse, transgene expression is found within 2 h in all major organs except the brain. The highest transgene activity is found in the lung (Fig. 2), predominantly in the pulmonary endothelial cells (4). Transgene expression is also found in metastatic tumor cells in the lung (5). The transgene expression peaks at about 8–24 h after injection and gradually declines to lower levels within 48–72 h. When a tumor suppresser gene (Rb) was delivered with LPD nanoparticles, it was observed that metastatic tumor cells in the lung underwent spontaneous apoptosis. This led to a significant reduction in the percentage of mice with lung metastasis after LPD-Rb gene but not LPD-control gene treatment (5). DC-Chol/DOPE LPD has been optimized for brain gene transfer by intracranial injection. A high level of transgene expression in the brain was detected for more than 10 months in rodents and at least at 1 month in primates. Two

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Fig. 2. Time-course of transgene expression following intravenous injection of LPD.

children with Canavan’s disease were given intraventricular administration of DC-Chol/DOPE LPD carrying the ASPA gene, and both showed clinical improvements (6). 1.4. Toxicity Intracranial injection of LPD has been shown to be safe in animals and in human patients without any noticeable side effects (6). However, systemic administration of LPD or liposome-plasmid DNA complex can trigger a proinflammatory cytokine response, which is dose dependent (7). Although the induction of cytokines (tumor necrosis factor-α [TNF-α], interleukin-12 [IL-12], IL-6, interferon-γ [IFN-γ], etc.) may be beneficial for the treatment of tumors (8,9), these cytokines are toxic to the injected animals at high doses. Furthermore, these cytokines inhibit transgene expression (7,10). Recent studies have revealed that the induction of proinflammatory cytokine is largely due to the unmethylated CpG dinucleotides that are present in the bacterial plasmid DNA (7). Ways to overcome this problem include modification of plasmid DNA to reduce the number of CpG motifs (11), use of a polymerase chain reaction (PCR) fragment instead of the intact plasmid (12), and the use of a general immunosuppressant such as dexamethasone (10).

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2. Materials 2.1. Preparation of LPD Complex 1. 2. 3. 4. 5.

50-mL polypropylene conical tube. 1.5-mL Eppendorf tube. Dextrose (Sigma). Sterile water (autoclaved and 0.2-μm-pore sterile-filtered) Cationic liposomes, prepared as described in the protocol (see Subheading 3.2). a. 10 mg/mL (14.3 mM) DOTAP/Chol liposome b. 2 mM DC-Chol/DOPE liposome (see Note 2). 6. 1 mg/mL plasmid DNA in sterile water (see Note 3). 7. 10 mg/mL protamine sulfate USP (Elkins-Sinn, Cherry Hill, NJ). 8. 5X Dextrose (26.0% [w/v]), 100 mL. Dissolve 13 g dextrose in approximately 40 mL sterile water, and then bring to 50 mL with sterile water. Sterile filter the solution through a 0.2 μm membrane and store at room temperature for up to 1 year.

2.2. Liposome Preparation by Thin-Film Hydration followed by Extrusion 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12.

N2 gas tank. Vacuum dessicator. Bath sonicator. 30.0-mL Corex glass centrifuge tube (or any clean glass tube). Sterile water. 25.0 mg/mL DOTAP stock solution in chloroform (Avanti Polar Lipids, Alabaster, AL). 20.0 mg/mL cholesterol stock solution in chloroform. 2.0 mg/mL DC-Chol stock solution (3.72 mM DC-Chol) in chloroform. 20.0 mg/mL DOPE stock solution in chloroform (Avanti Polar Lipids, Alabaster, AL). LiposoFast™ extruder, with 1.0-mL syringes (Avestin, Ottawa ON, Canada). 1.0, 0.4, and 0.1 μm Nuclepore® polycarbonate membrane filters (Corning®, available from VWR). Cholesterol (20 mg/mL in chloroform), 5 mL Weigh 100 mg cholesterol into a glass test tube previously rinsed 3× with chloroform and dried. Dissolve in approximately 4 mL chloroform. Bring to 5 mL with chloroform. Store at –20°C in capped and sealed glass container.

3. Methods 3.1. Preparation of LPD Complex 1. Volumes and quantities are for 100 μg of plasmid DNA in a final volume of 600 μL (DOTAP/Chol liposome) or 400 μL (DC-Chol/DOPE liposomes). For larger doses, volumes and quantities should be proportionately scaled up (see Fig. 3 for illustration of the steps).

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Fig. 3. Preparation of liposome-polycation-DNA (LPD).

2. a. For DOTAP/Chol liposomes prepare liposome/polycation (LP) solution in a 50-mL conical tube by adding 60 μL 5X dextrose, 148.2 μL sterile water, 86 μL DOTAP liposomes, and 6 μL protamine sulfate. Mix by vortexing at medium speed for 10 s. b. For DC-Chol/DOPE liposomes, prepare LP solution in a 50-mL conical tube by adding 40 μL 5X dextrose, 122 μL sterile water, 30 μL DC-Chol/DOPE liposomes, and 8 μL protamine sulfate. Mix by vortexing at medium speed for 10 s. 3. a. Make up a DNA solution (D solution for DC-Chol/DOPE liposomes) in an eppendorf tube by adding 60 μL 5X dextrose, 140 μL sterile water, and 100 μL plasmid DNA. Gently tap tube to mix. Do not vortex. b. Make up a DNA solution (D solution for DOTAP-chol liposomes) in an eppendorf tube by adding 40 μL 5X dextrose, 60 μL sterile water, and 100 μL plasmid DNA. Gently tap tube to mix. Do not vortex. 4. While gently swirling LP solution, slowly add D solution dropwise. It takes about 5–10 s to add 300–400 μL of D solution. A tip with a wide opening to transfer the D solution is recommended, such as the 1000-μL pipet tip or plastic transfer pipet (see Note 4). 5. Incubate the complex at room temperature for 10–15 min prior to injection to allow for complex maturation.

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3.2. Preparation of Liposomes by Thin-Film Hydration followed by Extrusion Thin-film hydration followed by extrusion is one of many methods that can be used to prepare liposomes. This method was selected because it provides a quick and easy protocol for the preparation of a concentrated and homogeneous suspension of small unilammellar liposomes suitable for laboratory-scale animal experiments. The method involves forming a thin film of dried lipids on the bottom of a glass tube. The lipids are then hydrated in a desired aqueous solution (e.g., water or 5.2% dextrose) to form a suspension of mixed, multilammelar liposomes. Extrusion is a method of liposome preparation whereby lipid suspensions are pushed through polycarbonate filters of desired pore size. The shear force produced by passage of the lipids through the pores results in the formation of liposomes with unilamallar lipid bilayers. The size of the resultant liposomes can be dictated, in part, by choosing the appropriate pore size of the filters used during extrusion. It should be noted that for largescale preparation of liposomes, microfluidization is the method of choice (13). The preparation of DC-Chol/DOPE liposome (2 mM DC-Chol) DOTAP/ Chol liposome (14.3 mM DOTAP = 10 mg/mL DOTAP) stock solutions is described below. A cationic liposome preparation with a 3:2 molar ratio of DC-Chol/DOPE represents the optimal formulation to be used in LPD for intracranial injection. The optimal liposome preparation to be used in LPD for systemic injection is composed of a 1:1 molar ratio of DOTAP/cholesterol. Both cationic liposome stock solutions are stable for several months when stored at 4°C. 3.2.1. Preparation of Thin Film 1. Rinse a 30-mL Corex tube 3× with chloroform. There is no need to dry the residual chloroform since it will be evaporated in step 3. 2. Mix desired amount of lipids in the glass tube. a. For 2 mL of 10 mg/mL DOTAP/cholesterol liposomes (1:1 molar ratio), mix 0.8 mL DOTAP (mol wt 698.6) stock solution and 0.55 mL cholesterol (MW386.7) stock solution. b. For 2 mL of 2 μmol/mL DC-chol/DOPE liposomes (3:2 molar ratio), add 1.07 mL DC-Chol stock solution and 0.1 mL DOPE stock solution and mix. 3. In a chemical hood, evaporate chloroform to form a thin lipid film on the glass by blowing N2 gas down the side of the tube while rotating the tube. This process should be done in a chemical hood. The chloroform fume is hazardous. To speed up the process, the tubes can be dipped in a warm water bath. 4. Dry film to completion by vacuum desiccation for 2–3 h (see Note 5). To prevent loss of lipid film under vacuum, cover tube with aluminum foil and poke small holes in the foil with a needle.

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3.2.2. Hydration of the Thin Film 1. Add 2 mL of sterile water to film. 2. Suspend lipids in solution by vortexing for 15 s on maximum speed several times. Lipids may remain on the side of the tube, appearing as a solid, white precipitate. Several quick (10–15 s) bursts in a bath sonicator will help to suspend the lipids in solution. 3. Incubate suspension either at room temperature for 2–3 h or at 4°C overnight to allow for complete hydration of lipids. It is our experience that the longer the hydration, the easier the extrusion. Overnight hydration is recommended for common practice, and 48 h of hydration is also acceptable.

3.2.3. Extrusion 1. Vortex the lipid suspension and heat it for 5–10 min in a 65°C water bath. Should you observe any lipid aggregates, sonicate the suspension in a bath sonicator until all aggregates disappear, and then return to water bath. 2. Place two 1.0-μm polycarbonate filters in the extruder. 3. Heat the extruder to 65°C for 5 min. Heating the lipid suspension and the extruder to 65°C maintains the lipids in a liquid state. This allows for easier extrusion and improved lipid mixing. 4. Extrude the lipid dispersion by passing the suspension through the extruder 5×. Return the extruder to the water bath. Following extrusion, the lipid suspension should be transformed from an opaque, cloudy solution to a transluscent suspension. 5. Repeat steps 2–4 using 0.4- and 0.1-μm polycarbonate filters sequentially to obtain small unilamellar liposomes with a mean diameter of 100–200 nm. 6. Store liposomes at 4°C.

4. Notes 1. A variety of cationic liposome formulations are commercially available for lipofection of cells in tissue culture. Optimal formulations are highly cell line dependent and typically do not correlate with optimal formulations used for gene transfer of corresponding tissues in vivo. Thus, for in vitro transfection, the reader is advised to test a variety of the commercially available liposomes following the manufacture’s instructions. 2. The DOTAP/Chol liposome is made of a 1:1 molar ratio of DOTAP and cholesterol. Each DOTAP molecule carries a positive charge, and cholesterol is neutral. In gene transfer studies, one often needs to calculate the amount of DOTAP according to different charge ratio requirement. Thus, for convenience, the DOTAP/Chol liposome solution is labeled as 10 mg DOTAP/mL; it also contains 5.5 mg Chol/mL. For DC-Chol/DOPE liposomes, the stock solution is 2 mM of total lipids, i.e, 1.2 mM of DC-Chol and 0.8 mM of DOPE. 3. Plasmid DNA shall be highly purified and endotoxin free (e.g., using DoubleCsCl gradient purification or Endofree™ plasmid/cosmid purification kits avail-

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able from QIAGEN®). In addition, it is required that plasmid DNA (or other forms of DNA) be dissolved in water or 5.2% dextrose solution. This is because salt interferes with the charge-charge interaction between DNA and cationic lipid or polymer and causes the formation of aggregates. 4. White, string-like precipitates may form during mixing. This is most commonly caused by salt in the solutions (TE, NaCl, etc.) The precipitates appear to be toxic to mice following iv injection. Proper contour of the mixing vessel (i.e., the 50mL conical tube), swirling of the LP solution, and dropwise addition of the D solution help to prevent the formation of the precipitate. If the precipitate forms, it is not advised to proceed with injection. Instead, try preparing the complex again. With practice, precipitate formation can routinely be avoided. Again, never vortex the complex since it contains plasmid DNA. 5. For the preparation of liposomes by the thin-film hydration followed by extrusion method, one should allow 3–4 h for the formation of the dry film, 2–3 h or overnight for hydration of the lipids, and 1–2 h for extrusion. For preparation of LPD, one should allow 1/2–1 h.

References 1. Gao, X. and Huang, L. (1996) Potentiation of cationic liposome mediated gene delivery by polycations. Biochemistry 35, 1027–1036. 2. Sorgi, F. L., Bhattacharya, S., and Huang, L. (1997) Protamine sulfate enhances lipid mediated gene transfer. Gene Ther. 4, 961–968. 3. Li, B., Li, S., Tan, Y., et al. (2000) Lyophilization of cationic lipid-protomineDNA (LPD) complexes. J. Pharm. Sci. 89, 355–364. 4. Li, S. and Huang, L. (1997) In vivo gene transfer via intravenous administration of cationic lipid/protamine/DNA (LPD) complexes. Gene Ther. 4, 891–900. 5. Nikitin, A. Y., Juarez, M. I., Li, S., Huang, L., and Lee, W. H. (1999) RB-mediated suppression of spontaneous multiple endocrine neoplasia and lung metastases in Rb+/- mice. Proc. Natl. Acad. Sci USA 96, 3916–3921. 6. Leone, P., Janson, C.G., Bilianuk, L., et al. (2000) Aspartoacylase gene transfer to the mammalian central nervous system with therapeutic implications for Canavan disease. Ann. Neurol. 48, 27–38. 7. Li, S., Wu, S.P., Whitmore, M., et al. (1999) Effect of immune response on gene transfer to the lung via systematic administration of cationic lipidic vectors. Am. J. Physiol. Lung Cell. Mol. Physiol. 276, L796–L804. 8. Hofland, H. and Huang, L. (1995) Inhibition of human ovarian carcinoma cell proliferation by liposome-plasmid DNA complex. Biochem. Biophys. Res. Commun. 207, 492–507. 9. Whitmore, M., Li, S., and Huang, L. (1999) LPD lipopolyplex initiates a potent cytokine response and inhibits pulmonary tumor growth. Gene Ther. 6, 1867–1875. 10. Tan, Y., Li, S., Pitt, B., and Huang, L. (1999) The inhibitory role of CpG immunostimulatory motifs in cationic lipid vector-mediated transgene expression in vivo. Hum. Gene Ther. 10, 2153–2161.

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11. Yew, N. S., Zhao, H., Wu, I. H., et al. (2000) Reduced inflammatory response to plasmid DNA vectors by elimination and inhibition of immunostimulatory CpG motifs. Mol. Ther. 1, 255–262. 12. Hofman, C. R., Dileo, J. P., Li, Z., Li, S., and Huang, L. Efficient in vivo gene transfer by PCR amplified fragment with reduced inflammatory activity. Gene Ther., 8, 71–74. 13. Sorgi, F. L. and Huang, L. (1996) Large scale production of DC-Chol liposomes by microfluidization. Int. J. Pharmaceut. 144, 131–139.

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7 Solvoplex Synthetic Vector for Intrapulmonary Gene Delivery Preparation and Use Klaus Schughart and Ulla B. Rasmussen

1. Introduction For in vivo gene transfer, synthetic (nonviral) vectors are thought to have several advantages compared with viral vectors: they can accommodate largesize DNA molecules (therapeutic genes including their endogenous regulatory regions), be used under reduced confinement conditions, be administered repeatedly, and be modified with appropriate ligands that allow specific cell targeting. Until now, many different types of organic compounds have been tested as synthetic gene delivery vectors in animal models by various routes of administration (reviewed in refs. 1–13). Intrapulmonary gene delivery represents an important route of administration for treatment of monogenic or multifactorial diseases like cystic fibrosis and asthma. Furthermore, gene delivery via the intrapulmonary route would be an attractive noninvasive delivery method for systemic expression of therapeutic proteins by targeting alveolar cells, which then express and secrete the gene products into the bloodstream. Different synthetic vectors have been studied for their potential use as gene transfer vectors to achieve expression after intrapulmonary delivery; some of them have been evaluated in clinical studies (reviewed in refs. 14–17). Recently, we described a new type of synthetic vector, named solvoplex, which is based on organic solvents and which can greatly enhance gene delivery to the lung epithelium after intrapulmonary delivery (18). Solvoplexes repFrom: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. DPSO solvoplexes are more efficient than DNA alone, DOTAP lipoplexes, or PEI polyplexes. Female B6SJLF1 mice were injected IT with solvoplexes, DNA alone, lipoplexes, or polyplexes (25 μg/50 μL of plasmid pTG11033 in each case; for details, see ref. 18), and luciferase expression in lung homogenates was determined 1 day after injection. As control, naive mice (not injected) were analyzed. (+/–) refers to the N/P molar ratio of lipid or polycation to DNA in lipo- and polyplexes (21). Mean values were calculated and statistical analyses were performed using the MannWhitney rank sum test. *, p < 0.04 in a pairwise comparison of the lipoplexes and polyplexes to DPSO solvoplexes. n, number of mice analyzed in each group. (From ref. 18 with permission.)

resent highly efficient gene transfer vectors to target the lung airway epithelium in mice and rats after intrapulmonary delivery, they are easy to prepare and stable for weeks, and they can be readministered. Here we describe the preparation and use of solvoplex vectors for preclinical studies in rodents. 1.1.

Characteristics of Solvoplex Vectors

Solvoplex vectors represent easy to prepare mixtures of plasmid DNA and organic solvents. Among several polar aprotic solvents tested for efficacy of intrapulmonary gene delivery after intratracheal (IT) injection in mice, di-npropylsulfoxide (DPSO), dimethylsulfoxide (DMSO), tetramethylurea (TMU), and butylmethylsulfoxide (BMSO) solvoplexes yielded the highest luciferase reporter gene expression in the lung. The best results were obtained with


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Fig. 2. LacZ reporter gene expression is observed in the lung airway epithelium after IT injection of solvoplexes. Lungs were prepared 1 day after IT injection of female B6SJLF1 mice, stained with X-Gal, and cut into large pieces; then the cut open surface was photographed under a dissection microscope. (A) Noninjected control mice. (B) Mice injected with 15% DPSO solvoplexes (50 μg/50 μL of pTG11034 plasmid DNA). Lungs from 15% DPSO solvoplex-injected mice were embedded in paraffin, sectioned, mounted, and viewed under the light microscope using (C) Nomarski or (D) brightfield illumination after H&E staining. Arrows indicate examples of LacZpositive (blue-stained) cells. (From ref. 18 with permission.)

solvoplexes containing 15% DPSO (18). At this concentration, up to 400-fold increased expression levels were obtained when compared with DNA alone (“naked DNA”) (Fig. 1). In addition, diethylsulfoxide (DESO), methylethylsulfoxide (MESO), propylenglycol (PPG), tetramethylensulfoxide (TEMSO), and sulfolane resulted in lower levels of gene expression but still higher than with DNA alone. Compared with dioleoyl-trimethylammonium propane/ dioleoylphosphatidylethanolamine (DOTAP/DOPE), DOTAP/cholesterol lipoplexes, or polyethyleneimine (PEI) polyplexes, increases of 260-, 25-, or 4-fold, respectively, were observed with DPSO solvoplexes (Fig. 1). Thus, solvoplexes represent more efficiently performing vectors for intrapulmonary gene delivery than many of the currently used synthetic vectors. Also in rats, IT delivery of 15% DPSO solvoplexes resulted in gene expres-

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Fig. 3. Readministration of solvoplexes results in gene expression levels similar to single administration. Female B6SJLF1 mice were injected IT with solvoplexes (50 μg/25 μL of plasmid pTG11033) or with 1 ¥ 10E8 PFU AdTG8509 adenovirus (Ad) and analyzed for luciferase expression 1 or 29 days later. Two groups were reinjected with solvoplexes or with adenovirus at day 28, and 1 day later, luciferase expression in lung homogenates was determined. Mean values were calculated, and statistical analyses were performed using the Mann-Whitney rank sum test. *, p < 0.01 in a pairwise comparison of expression levels of adenovirus-injected mice analyZed after 29 days and reinjected mice, with mice analyzed at day 1. n, number of mice analyzed in each group. SEM: standard error of mean. (From ref. 18 with permission.)

sion in the lung (18). An important parameter for the clinical and preclinical use of synthetic vectors is the stability of complexes upon storage. When DPSO solvoplexes were kept at –20°C or at room temperature, no degradation of DNA was observed within a period of 15 days, and no loss in transfection efficiency of the DNA was noted (18). Furthermore, reporter gene expression in the lung could be observed after delivery of solvoplexes as a spray using a hand-held, high-pressure microsprayer device (IA-1C Intrapulmonary Aerosolizer; PennCentury) (18). 1.2. Gene Expression in the Lung Airway Epithelium Individual cells in the lung expressing a foreign gene can be localized after solvoplex delivery of LacZ or GFP reporter genes. For example, in mice injected with 15% DPSO solvoplexes, LacZ-positive cells were detected in the epithelium of the proximal regions of the lung airways (Fig. 2).


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1.3. Readministration of Solvoplex Vectors Gene expression after solvoplex delivery was highest on day 1 after injection and declined rapidly until day 7, when expression levels were only slightly above background. Thus, when prolonged gene expression is needed, readministration will be required. We observed that, in contrast to first-generation adenovirus vectors, after a second administration of 15% DPSO solvoplexes, expression levels could be obtained that were equivalent to the levels seen after the first injection (Fig. 3). 1.4. Toxicity of Solvoplexes Administration of solvoplexes resulted in pathologic changes in the lung at 1 day after injection that were not significantly different from the changes observed after delivery of DNA alone. Seven days after injection, no or only very weak residual inflammation was seen for solvoplexes and DNA alone. Changes in relative body weight or serum transaminase levels were not significantly different between injected and noninjected mice. It should also be noted that the amount of DPSO applied in our protocol is 5000-fold below the median lethal dose (LD50) determined for mice after intraperitoneal injection (19). 1.5. Mechanism of Transfection The mechanism of transfection of airway epithelial cells by solvoplexes is currently unknown. It is conceivable that organic solvents change the composition of the cell membrane by altering its fluidity or the properties and distribution of receptors and that such changes enhance DNA uptake. Also, it is possible that the basolateral cell surfaces of epithelial cells in the lung become exposed in the presence of solvent because the solvent weakens cell-cell interactions, thus allowing DNA uptake also via the basolateral membrane. In addition to effects at the cellular level, the conformation of DNA may be altered in the presence of solvents in such a way that its uptake is facilitated. 1.6. Conclusion and Perspectives Our results demonstrate the use of solvoplexes as an attractive alternative and complementary gene delivery vehicle to the currently available gene transfer vectors, especially for preclinical studies. They result in high levels of gene expression in the lung airway epithelium, and they are easy to prepare, stable over time, and of moderate toxicity; they can also be readministered. However, before solvoplexes could be used in the clinic, several issues, especially those concerning potential local pathogenic effects and improved delivery methods, must be addressed in more detail.

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2. Material 2.1. Solutions 1. Phosphate buffered saline (PBS): 2 mM KH2PO4, 8 mM Na2HPO4, 150 mM NaCl. 2. X-Gal staining solution: 5 mM K3Fe(CN)6, 5 mM K4Fe(CN)6, 2 mM MgCl2, 1 mg/mL X-Gal, 0.02% NP-40, 0.01% Na-deoxycholate in PBS. 3. Anesthetic mixture for mice: 5.2 mL 0.15 M NaCl, 1 mL Imalgene 1000 (ketamine; Merial, Lyon, France), 0.5 mL 2% Rompun (xylazine; Bayer, Leverkusen, Germany). 4. Anesthetic mixture for rats: 5 mL Imalgene 1000 (ketamine), 1.5 mL 0.5% Vetranquil (acepromazine; Sanofi-Santé-Nutrition Animale, Libourne, France).

2.2. Solvents for Solvoplexes 1. TMU was obtained from Sigma (L’Isle d’Abeau Chesnes, France; cat. no. T3875). 2. BMSO was synthesized by oxidation of methylbutylsulfide (Lancaster, Strasbourg, France; cat. no. 12039) with NaIO4 (Sigma; cat. no. S1147). 3. DMSO was purchased as tissue culture grade from Sigma (cat. no. D2650). 4. DPSO could not be obtained commercially in a pure enough form and was thus synthesized by oxidation of di-n-propylsulfide with NaIO4 (see Subheading 3.2.).

2.3. Expression Plasmids The expression plasmid pTG11033 contained the luciferase gene under control of the IE1-CMV promoter, intron 1 of the HMGCoAR gene, and the SV40 polyA signal. Plasmid pTG11034 contained the bacterial LacZ gene with a nuclear localization signal under control of the IE1-CMV promoter, the rabbit ß1-globin ivs2 intron, and SV40 polyA. Plasmid pEGFP-C1 (Clontech, Palo Alto, CA) contained the GFP gene under control of the IE1-CMV promoter. 2.4. Mice and Rats Female C57BL/6 and B6SJLF1 mice (8–10 weeks old) and female SpragueDawley (OFA-SD) rats (approx 100 g) were obtained from authorized suppliers (Iffa Credo, l’Arbresle, France; Charles River, St. Germain sur l’Arbresle France; Janvier, Le Genest, France) as special pathogen-free (SPF) grade animals (see Note 1). They were housed under SPF conditions and according to the French regulations for animal experimentation. After arrival, animals were allowed at least 1 week to recover from transport and adapt to the environment before the beginning of the experiments.


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3. Methods 3.1. Preparation of DNA Plasmid DNA is prepared by the alkaline lysis method (20) from cultures grown in Erlenmeyer flasks or fermenters. Plasmid DNA is then precipitated by isopropanol, and the pellet is washed with 70% ethanol. Crude plasmid preparations are then purified by two subsequent CsCl density gradient centrifugations (20). 1. Harvest the plasmid band from the second CsCl density gradient (about 8 mL of solution). 2. Extract ethidiumbromide 4–5× with 5 mL butanol (saturated with water/CsCl). 3. Dialyze against TE. 4. Digest RNA by adding, for 8 mL of plasmid solution, 10 μL of an RNAase solution (10 mg/mL in water). 5. Incubate for 30 min at 37°C and add 80 μL 10% sodium dodecyl sulfate (SDS) and 10 μL of proteinase K (10 mg/mL in water). 6. Incubate at 37°C for 2 h and stop reaction by incubation at 65°C for 5 min. 7. Extract plasmid solution twice with dichlormethan. 8. Precipate DNA by adding 1/10 vol of 3 M Na-acetate, pH 5.0, and 2.5 vol of 99.9% ethanol; wash pellet 3X with 70% ethanol. 9. Dissolve DNA in TE to a final concentration of 1 mg/mL or less. 10. Extract endotoxins by adding 1/9 vol of 3 M Na-acetate, pH 5.0 and then 1/9 vol of 10% TX114 (Sigma; cat. no. T-7003) in 0.3 M Na-acetate, pH 5.0, vortex for 1 min, incubate on ice for 10 min, vortex for 3 s, incubate at 42°C for 5 min, centrifuge for 10 min at 37°C at 2200g, and transfer aqueous phase to new tube; repeat twice. 11. Precipitate DNA by adding 2.5 vol ethanol, incubate for 2 h at –20°C, wash the pellet 3× with 70% ethanol,and dry the pellet for 5 min in a lyophylizator. 12. Dissolve DNA in TE. 13. Determine DNA concentration and purity by measuring OD260 and OD280 (20). 14. Determine endotoxin concentration by using the LAL Coatest Endotoxin kit (Biogenic, Maurin, France). For use in animals, endotoxin concentrations should be 10% of solvent are more viscous than water and need to be injected very slowly. If you are not very experienced with IT injections, the results may vary considerably between individual animals in the beginning. 7. Maximal expression levels were observed 1 day after injection. The peak of expression may be slightly earlier than 24 h; we did not investigate this in detail. 8. After solvoplex injection, we observed expression in both the lung and trachea, but expression levels were variable for the trachea. In the trachea, similar expression levels were seen for solvoplexes as for DNA alone, whereas in the lung, expression was much higher after solvoplex injection (Fig. 1). Thus, if one is interested in lung gene transfer, the lung should always be studied separately from the trachea. 9. RLU can be converted into the corresponding mass (ng) of luciferase protein produced by preparing standard curves with purified commercially available luciferase. In this case, it is necessary to generate a standard curve at the same time as samples are being analyzed. However, be aware that the conversion depends on the purity of the luciferase protein batch used for the standard curve and that this can vary between batches and suppliers. Therefore, even though the conversion of RLU to ng luciferase protein allows a better comparison of expression levels between laboratories, it is not an “absolute” value. 10. For better fixation of the tissues, mice can be deeply anesthesized and perfused with PBS and then 2% formaldehyde; isolated organs can be fixed in this solution for 30–60 min at room temperature. 11. Histologic staining of all sections is not recommended, because the LacZ staining could be masked. We prefer to leave one section unstained and to counterstain the neighboring section with haematoxylin and eosin (Merck) for visualization of morphologic structures. 12. Long working distance objectives are required.

5. Acknowledgments We acknowledge the excellent technical help of D. Ali Hadji, J. Kintz, M. de Meyer, H. Schultz, M. Dupont, F. Mischler, D. Elmlinger, C. Mougin, N. Accart, and V. Nourtier; Dr. B. Cavallini and I. Renardet for preparing plasmid DNAs; and Drs. R. Bischoff, F. Perraud, O. Boussif, N. Silvestre, Y. Cordier, A. Pavirani, and H.V.J. Kolbe for their contributions to the development and characterization of solvoplex vectors. We thank Dr. M. Courtney for critical comments on the manuscript. This work was supported in part by the AFM (Association Française contre les Myopathies) and the AFLM (Association Française de Lutte contre la Mucoviscidose). References 1. Abdallah, B., Sachs, L., and Demeneix, B. (1995) Non-viral gene transfer: applications in developmental biology and gene therapy. Biol. Cell. 85, 1–7.

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2. Felgner, P. L., Tsai, Y. L., Sukhu, L., et al. (1995) Improved cationic lipid formulations for in vivo gene therapy. Ann. N.Y. Acad. Sci. 772, 126–139. 3. Hagstrom, J. (2000) Self-assembling complexes for in vivo gene delivery. Curr. Opin. Mol. Ther. 2, 143–149. 4. Hutchins, B. (2000) Characterization of plasmids and formulations for non-viral gene therapy. Curr. Opin. Mol. Ther. 2, 131–135. 5. Lollo, C., Banaszczky, M., and Chiou, H. (2000) Obstacles and advances in nonviral gene delivery. Curr. Opin. Mol. Ther. 2, 136–142. 6. Lee, R. J. and Huang, L. (1997) Lipidic vector systems for gene transfer. Crit. Rev. Ther. Drug Carrier Syst. 14, 173–206. 7. Li, S. and Huang, L. (2000) Nonviral gene therapy: promises and challenges. Gene Ther. 7, 31–34. 8. Luo, D. and Saltzman, W. M. (2000) Synthetic DNA delivery systems. Nat. Biotechnol. 18, 33–37. 9. Kabanov, A., Felgner, P., and Seymour, L. (1998) Self-Assembling Complexes for Gene Delivery. John Wiley & Sons, Chichester, UK. 10. Mahato, R. I., Rolland, A., and Tomlinson, E. (1997) Cationic lipid-based gene delivery systems: pharmaceutical perspectives. Pharm. Res. 14, 853–859. 11. Rolland, A. P. (1998) From genes to gene medicines: recent advances in nonviral gene delivery. Crit. Rev. Ther. Drug Carrier Sys. 15, 143–198. 12. Schaffer, D. and Lauffenberger, D. (2000) Targeted synthetic gene delivery vectors. Curr. Opin. Mol. Ther. 2, 155–161. 13. Scherman, D., Bessodes, M., Cameron, B., et al. (1998) Application of lipids and plasmid design for gene delivery to mammalian cells. Curr. Opin. Biotechn. 9, 480–485. 14. Alton, E. W., Geddes, D. M., Gill, D. R., et al. (1998) Towards gene therapy for cystis fibrosis: a clinical progress report. Gene Ther. 5, 291–292. 15. Korst, R. J., Mcelvaney, N. G., Chu, C. S., et al. (1995) Gene therapy for the respiratory manifestations of cystic fibrosis. Respir. Crit. Care Med. 151, S75–S87. 16. Flotte, T. (1999) Gene therapy for cystic fibrosis. Curr. Opin. Mol. Ther. 1, 510–615. 17. Rosenfeld, M. A. and Collins, F. S. (1996) Gene therapy for cystis fibrosis. Chest 109, 241–252. 18. Schughart, K., Bischoff, R., Rasmussen, U. B., et al. (1999) Solvoplex: a new type of synthetic vector for intrapulmonary gene delivery. Hum. Gene Ther. 10, 2891–2905. 19. Tatken, R. L. and Lewis Sr., J. R. (1983) Registry of Toxic Effects of Chemical Substances. Tractor Jitco, Rockville, MD. 20. Sambrook, J., Fritsch, E., and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. 21. Zanta, M. A., Boussif, O., Adib, A., and Behr, J. P. (1997) In vitro gene delivery to hepatocytes with galactosylated polyethylenimine. Bioconjug. Chem. 8, 839–844.

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8 Gene Correction Frequency by Chimeric RNA-DNA Oligonucleotide Using Nuclear Extracts Olga A. Igoucheva and Kyonggeun Yoon 1. Introduction Site-specific correction of single-base mutations in target DNA sequences has been developed using an RNA-DNA hybrid oligonucleotide (RDO) to correct or cause a specific point mutation in episomal and genomic DNA (1–14). In its original design, an RDO was composed of two strands, one strand containing both RNA and DNA (RNA-containing strand) and the other strand fully complementary to the RNA-containing strand but consisting of all DNA (DNAcontaining strand; Fig. 1). The RNA was incorporated because an RNA-DNA hybrid duplex is more active than a DNA duplex in homologous recombination by the RecA and Rec2 proteins (15,16). To render the oligonucleotide resistant to the RNaseH, ribose sugars were 2'-O-methylated, and to protect the 5' and 3' ends, a five GC clamp was placed at each end of the molecule. This original RDO molecule was empirically designed and has been modified subsequently. Recent RDO designs include a complete sequence complementarity of the RNA-containing strand to target DNA, a replacement of the central five DNA residues with 2'-O-methyl RNA, a placement of mismatch in the DNA-containing strand, and a chemical modification of the hairpin loops. These modifications result in a 3- to 10-fold increase in gene correction activity (17,18). These results suggest that two different functions could be imparted to two strands of RDO: the RNA-containing strand stabilization of a labile intermediate and the DNA-containing strand for strand pairing and directing DNA repair activity.

From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. The structure of RDO. RDO consists of RNA- and DNA-containing strands linked by a double T-loop and a 5-bp GC clamp. The RNA-containing strand has 10 2'-O-methyl RNA residues (R) flanking either side of a 5-residue DNA (D) stretch, which contains the base change desired for the mutation. The sequence of the RNAcontaining strand is complementary to the targeted DNA over a stretch of 25 residues except for a single mismatch (A:C) to the targeted base to be altered. The DNA-containing strand is complementary to the RNA-containing strand.

1.1. Standardized System for Measuring Gene Conversion The general application of RDO technology has been hampered by the lack of a standardized system to measure gene conversion in a particular cell type in a rapid and reproducible manner. For this purpose, we have constructed a shuttle vector, pCH110-G1651A, to measure the targeted gene correction of the mutant E. coli β-galactosidase gene (19). The mutant plasmid contained a single-base-point mutation at position 1651 (G→A) in the plasmid pCH110, which encodes the full-length E. coli β-galactosidase gene under the control of the SV40 early promoter. This mutation causes a Glu→Lys substitution in the Mg2+ binding site (amino acid 461) and results in a complete loss of catalytic activity. A shuttle vector whereby a gene product is expressed in both mammalian and bacterial cells makes it possible to transfer the conversion event mediated by the RDO in mammalian cells to bacteria for further analysis (Fig. 2). The advantage of this scheme is that, in bacteria, gene correction events can be rapidly and unambiguously scored, as blue colonies. We also established an in vitro system in which nuclear extracts from mammalian cells were shown to process RDO-mediated gene correction of the mutant β-galactosidase plasmid (19). This in vitro reaction was utilized to compare frequencies of gene conversion among cell lines (19) and to optimize the design of RDO (17). 1.2. Variation in Gene Correction Frequency among Different Cell Types We found a large variation in gene conversion frequencies among different cell types (5,19). Neither uptake nor nuclear stability of the oligonucleotide

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Fig. 2. Strategy of gene correction by RDO, an episomal transfection, and in vitro reaction with mammalian nuclear extracts, using the shuttle plasmid pCH110-G1651A containing a point mutation (G→A) in the E. coli β-galactosidase gene.

appears to be a limiting factor in our experiments, as measured by a radiolabeled or a fluorescein-conjugated oligonucleotide (5). Variable frequencies among different cell types are not surprising since each cell type is likely to have different rates of recombination and mismatch repair. However, it has been difficult to predict whether RDO technology can be applied to a particular cell type. Using the in vitro reaction, we measured the gene correction frequency of the mutant β-galactosidase shuttle vector. The frequency of gene conversion of

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Table 1 Frequency of In Vitro Gene Correction by RDO in Different Cell Types

Cell type

RDO

Molar ratio or RDO/mutant plasmid

CHO-K1 HeLa HaCaT PKC p53–/– p53+/+ p53+/+b DT40

β-Gal B β-Gal B β-Gal B β-Gal B β-Gal B β-Gal B β-Gal B β-Gal B

1000 1000 1000 1000 1000 1000 1000 1000

No. of Lac– colonies

No. of Lac+ colonies

% Lac+/Lac– a

4.0 × 103 34 × 103 28 × 103 110 × 103 6.9 × 103 26 × 103 0.6 × 103 15 × 103

5 1 1 2 53 0 5 12

0.1 0.003 0.004 0.002 0.8 400 mU/ mL. Within 5 days of the last mifepristone dose, EPO expression returned to undetectable levels. The 5-day mifepristone treatment triggered a substantial increase in hematocrit, with peak levels (57%) occurring 6 days following the final mifepristone dose. By day 30, 2 weeks after the final mifepristone dose, hematocrit returned to baseline levels, which was maintained at normal levels for an additional 20 days. The data demonstrate the ability of the muscle-specific GeneSwitch system to provide strict, ligand-dependent regulation of transgene expression in mice. The GeneSwitch systems for regulating erythropoietin and VEGF perform effectively in vivo at 1:1 ratios of the GeneSwitch and inducible plasmids. However, it is difficult to predict precisely the tightness of regulation that will be obtained with different transgenes, since sequence elements within the transgene itself can influence the strength of the inducible promoter. Thus, it may be necessary to modify the ratios of the two plasmids to refine the desired response. Delivery of plasmids to muscle by in vivo electroporation is associated with a transient period (approximately 30 days in length) during which localized regions of muscle damage and inflammation are evident. After approximately 30 days, the muscle tissue is normal in appearance, except for some evidence of recent myotube regeneration.

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8. The two components of the system, the GeneSwitch gene and the inducible transgene, can be combined as a cassette on one DNA molecule. When the single cassette was inserted into an adenovirus vector, highly effective regulation of growth hormone expression was observed in mice (27). However, when a single cassette is inserted into a plasmid, we typically observe a decline in the magnitude of drug-dependent transgene regulation due to increased basal expression of the inducible transgene. Thus, tight, drug-dependent regulation of transgene expression is best achieved with two separate plasmids.

References 1. Wolff, J. A., Ludtke, J. J., Acsadi, G., Williams, P., and Jani, A. (1992) Long-term persistence of plasmid DNA and foreign gene expression in mouse muscle. Hum. Mol. Genet. 1, 363–369. 2. Doh, S. G., Vahlsing, H. L., Hartikka, J., Liang, X., and Manthorpe, M. (1997) Spatial-temporal patterns of gene expression in mouse skeletal muscle after injection of lacZ plasmid DNA. Gene Ther. 4, 648–663. 3. Takeshita, S., Tsurumi, Y., Couffinahl, T., et al. (1996) Gene transfer of naked DNA encoding for three isoforms of vascular endothelial growth factor stimulates collateral development in vivo. Lab Invest. 75, 487–501. 4. Ulmer, J. B., Donnelly, J. J., Parker, S. E., et al. (1993) Heterologous protection against influenza by injection of DNA encoding a viral protein. Science 259, 1745–1749. 5. Mumper, R. J., Wang, J., Klakamp, S. L., et al. (1998) Protective interactive noncondensing (PINC) polymers for enhanced plasmid distribution and expression in rat skeletal muscle. J. Control. Release 52, 191–203. 6. Lemieux, P., Guerin, N., Paradis, G., et al. (2000) A combination of poloxamers increases gene expression of plasmid DNA in skeletal muscle. Gene Ther. 7, 986–991. 7. Shiotani, A., O’Malley, B. W. Jr., Coleman, M. E., Alila, H. W., and Flint, P. W. (1998) Reinnervation of motor endplates and increased muscle fiber size after human insulin-like growth factor I gene transfer into the paralyzed larynx. Hum. Gene Ther. 9, 2039–2047. 8. Neumann, E., Kakorin, S., and Toensing, K. (1999) Fundamentals of electroporative delivery of drugs and genes. Bioelectrochem. Bioenerg. 48, 3–16. 9. Mir, L. M. and Orlowski, S. (1999) Mechanisms of electrochemotherapy. Adv. Drug Deliv. Rev. 35, 107–118. 10. Somiari, S., Glasspool-Malone, J., Drabick, J. J, et al. (2000) Theory and in vivo application of electroporative gene delivery. Mol. Ther. 2, 178–187. 11. Smith, L. C. and Nordstrom, J. L. (2000) Advances in plasmid gene delivery and expression in skeletal muscle. Curr. Opin. Mol. Ther. 2, 150–154. 12. Aihara, H. and Miyazaki, J.-I. (1998) Gene transfer into muscle by electroporation in vivo. Nat. Biotechnol. 16, 867–870. 13. Mathiesen, I. (1999) Electropermeabilization of skeletal muscle enhances gene transfer in vivo. Gene Ther. 6, 508–514.

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14. Bettan, M., Emmanuel, F., Darteil, R., et al. (2000) High-level protein secretion into blood circulation after electric pulse-mediated gene transfer into skeletal muscle. Mol. Ther. 2, 204–210. 15. Rizzuto, G., Cappelletti, M., Maione, D., et al. (1999) Efficient and regulated erythropoietin production by naked DNA injection and muscle electroporation. Proc. Natl. Acad. Sci. USA 96, 6417–6422. 16. Mir, L. M., Bureau, M. F., Gehl, J., et al. (1999) High-efficiency gene transfer into skeletal muscle mediated by electric pulses. Proc. Natl. Acad. Sci. USA 96, 4262–4267. 17. Vicat, J. M., Boisseau, S., Jourdes, P., et al. (2000) Muscle transfection by electroporation with high-voltage and short-pulse currents provides high-level and long-lasting gene expression. Hum. Gene Ther. 11, 909–916. 18. Gossen, M. and Bujard, H. (1992) Tight control of gene expression in mammalian cells by tetracycline responsive promoters. Proc. Natl. Acad. Sci. USA 89, 5547– 5551. 19. Rivera, V. M., Clackson, T., Natesan, S., et al. (1996) A humanized system for pharmacological control of gene expression. Nat. Med. 2, 1028–1032. 20. No, D., Yao, T. P., and Evans, R. M. (1996) Ecdysone-inducible gene expression in mammalian cells and transgenic mice. Proc. Natl. Acad. Sci. USA 93, 3346– 3351. 21. Wang, Y., O’Malley, B. W. Jr., Tsai, S. Y., and O’Malley, B. W. (1994) A regulatory system for use in gene transfer. Proc. Natl. Acad. Sci. USA 16, 8180–8184. 22. http://www.geneswitch.com/ 23. Rendahl, K. G., Leff, S. E., Otten, G. R., et al. (1998) Regulation of gene expression in vivo following transduction by two separate rAAV vectors. Nat. Biotechnol. 16, 757–761. 24. Bohl, D., Salvetti, A., Moullier, P., and Heard, J. M. (1988). Control of erythropoietin delivery by doxocycline in mice after intramuscular injection of adenoassociated vector. Blood 92, 1512–1517. 25. Ye, X., Rivera, V. M., Zoltick, P., et al. (1999) Regulated delivery of therapeutic proteins after in vivo somatic cell gene transfer. Science 283, 88–91. 26. Hoppe, U. C., Marban, E., and Johns, D. C. (2000) Adenovirus-mediated inducible gene expression in vivo by a hybrid ecdysone receptor. Mol. Ther. 1, 159–164 27. Burcin, M. M., Schiedner, G., Kochanek, S., Tsai, S. Y., and O’Malley, B. W. (1999) Adenovirus-mediated regulable target gene expression in vivo. Proc. Natl. Acad. Sci. USA 96, 355–360. 28. Oligino, T., Poliani, P. L., Wang, Y., et al. (1998) Drug inducible transgene expression in brain using a herpes simplex virus vector. Gene Ther. 5, 491–496. 29. Abruzzese, R. V., Godin, D., Burcin, M., et al. (1999) Ligand-dependent regulation of plasmid-based transgene expression in vivo. Hum. Gene Ther. 10, 1499– 1507. 30. Abruzzese, R. V., Godin, D., Mehta, V., et al. (2000) Ligand-dependent regulation of vascular endothelial growth factor and erythropoietin expression by a plasmid-based autoinducible GeneSwitch system. Mol. Ther. 2, 276–287.

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31. Cheung, J. and Smith, D. F. (2000) Molecular chaperone interactions with steroid receptors: an update. Mol. Endocrinol. 14, 939–946. 32. Spitz, I. M., Bardin, C. W., Benton, L., and Robbins, A. (1998) Early pregnancy termination with mifepristone and misoprostol in the United States. N. Engl. J. Med. 338, 1241–1247. 33. http://www.fda.gov/cber/ptc/plasmid.txt Points to consider on plasmid DNA vaccines for preventive infectious disease indications, Food and Drug Administration, docket no. 96N-0400, December 1996.

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10 Photochemical Transfection Light-Induced, Site-Directed Gene Delivery Lina Prasmickaite, Anders Høgset, and Kristian Berg 1. Introduction Most nonviral gene transfection vectors deliver transfecting DNA into cells through the endocytic pathway (1,2). Poor escape from endocytic vesicles in many cases constitutes a major barrier for delivery of a functional gene, since the endocytosed transfecting DNA is unable to reach the cytosol and be further transported to the nucleus, but rather is trapped in endocytic vesicles and finally degraded in lysosomes (3). Therefore, the development of endosome-disruptive strategies is of great importance for the further progress of gene transfection. We have developed a new technology, termed photochemical internalization (PCI), to achieve light-inducible permeabilization of endocytic vesicles (4–8). The technology is based on photochemical reactions initiated by photosensitizers localized in endocytic vesicles and inducing rupture of these vesicles upon light exposure (4). This leads to the release of endocytosed macromolecules such as transfecting DNA from endocytic vesicles into the cytosol (Fig. 1). As a light-dependent treatment, PCI-mediated transfection (photochemical transfection) allows the possibility of directing the gene delivery to a desired site, e.g., achieving tumor-specific expression of a therapeutic gene in gene therapy in vivo. 1.1 Photosensitizers and Photochemical Reactions 1.1.1. General Principles Photosensitizers (S) are compounds that upon absorption of light become excited to an excited state (S*), which initiates further photochemical reacFrom: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Principle of photochemical internalization (PCI). I, endocytosis of the photosensitizer (S) and the transfecting gene (G); II, localization of the photosensitizer and the transgene in the same endocytic vesicles; III, rupture of endosomal membrane upon light exposure and subsequent release of the transfecting gene into the cytosol.

tions. The photochemical reactions may proceed via a type I process, with exchange of electrons between the photosensitizer and biomolecules, or a type II process, inducing formation of singlet oxygen (1O2). It is acknowledged that the photochemical reactions induced by the photosensitizers used in photodynamic therapy (PDT) and described here occur via type II reactions. Singlet oxygen is a highly reactive form of oxygen formed after interaction between the excited state of the photosensitizer (S*) and triplet ground-state molecular oxygen (3O2) (9,10). Schematically: 3O

2

1O

2

S + light→ S*

→oxidative reactions

Singlet oxygen can further oxidize various biomolecules such as unsaturated fatty acids, some amino acids, and guanine, inducing damage into various cellular structures (11). However, singlet oxygen has a very short lifetime (90%, the pools of the transduced 293/GPG, without selection, can be used directly as stable producer cells. 1. Day 1. Grow 293/GPG cells on 100-mm tissue culture dishes in DMEM medium with tetracycline, until 80% confluent. Trypsinize the cells and pass them in a 1:5 dilution. Culture overnight (15–18 h) at 37°C. 2. Day 2. Cells should be about 40–50% confluent. Thaw VSV-G/MuLV supernatant from transient transfection in 37°C water bath (requires 3 mL/100-mm plate), and add Polybrene (1:1000) to a final concentration of 8 μg/mL. Remove medium in the cell culture plate. Add the 3 mL supernatant to the plate and culture for 2 h at 37°C. 3. Add 10 mL DMEM with tetracycline to the virus-cell mixture plate. Culture overnight. 4. Day 3. Replace the medium with 10 mL fresh medium with tetracycline. Culture for 2–3 days until confluent. 5. Split the cells into five plates. Freeze the cells for later use or change medium into viral production medium to produce virus.

3.3. Generation of VSV-G/MuLV from a Producer Cell Line 1. Grow the producer cells (293/GPG/CnBgSN) to 80% confluent in maintenance medium. 2. Remove the medium and wash the cells with PBS once. Replace the medium with 6 mL production medium (without tetracycline), and culture overnight. 3. Collect the supernatant at 24 h, and replace with fresh 6 mL production medium. This can be repeated 3–4 times until most of the cells are detached and float up. This first collection has low virus titer (104–105 cfu/mL) and may be discarded.

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Yu Filter the following collections through a 0.45-μm filter and aliquot. The supernatant should have a virus content of about 106–107 cfu/mL.

3.4. Concentration of VSV-G/MuLV 1. Centrifuge the viral supernatant (100–500 mL) at 13,800g in a Beckman rotor JA-14 for 12 h. 2. The pellet is resuspended in 90% of the plasmid should be in linear form). This step should be performed in an RNase-free environment (preferably on a bench dedicated to RNA work, with clean pipets and other equipment). Removal of the DNA template or precipitation of RNA may not be crucial steps, but they are recommended since we have used them in our experiments. The manual of the SFV Gene Expression System indicates that in vitro synthesized RNA is suitable for electroporation without any purification steps. One reaction routinely yields 30–60 μg of purified RNA, and the typical A260/A280 ratio is about 2.2. Lower yields may indicate a poor-quality DNA template or problems with the kit. (Always include a control reaction, using the template pTRI-Xef1 from the kit.) The quality of the RNA can be checked on regular 1.5% agarose gel, using TAE or TBE buffer. However, RNA is vulnerable in this kind of environment and degrades rapidly. Use high voltage and a short time to verify the overall integrity of the RNA; accurate size determination under these conditions is not possible. (Denaturing RNA gel with formaldehyde is required for more precise analysis of the produced RNA species.) Some templates are more difficult to transcribe, resulting in low proportions of the full-length product and varying number of shorter RNA species. These are likely to be caused by premature runoff of the SP6 polymerase at difficult secondary structures of the template DNA. The amount of RNA for one electroporation is high, since the virus yields were directly proportional to the amount of SFV-RVC++ RNA (up to 50 μg). This is

Alphavirus/Retrovirus Hybrid Vector System

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probably because the RNA preparation consists of a mixture of different species and only up to 20% of it is full-length. Electroporation conditions depend on the equipment in use. It is recommended that other electroporators than the one we used be optimized for maximal efficiency and virus production. The number of pulses given (under indicated conditions) can also vary; we have observed that BHK-21 cells can take up to 4 pulses, but in this study only 3 pulses were used. The whole-virion dot-blot method is a rapid and easy way to get an estimate of the number of SFV-RVC++ virions in the preparation. There is no need for prior virion RNA purification, and different conditions for dot blotting and hybridization can be used. The sensitivity of this method is about 1000 SFV virions/mL, which is sufficient to give titers of any relevant virus preparation. We used an SFV-RVC++ MOI of 100 on PHOENIX cells, although even higher virus amounts can yield better retrovirus production. When adjusting the volume of activated SFV-RVC++ for retrovirus packaging cell plates, be aware of the possibility that too small volumes can evaporate significantly during the 90-min incubation and result in low retrovirus yield (due to damaged producer cells). The growth temperature (32°C) and incubation time (16 h) of PHOENIX cells are optimized for maximal production and minimal degradation of amphotropic retroviruses. Retroviral vectors with an inserted minigene (and promoterless Neo gene) cannot be titrated with the G418 resistance assay; use the dot-blot titration method described in Subheading 3.3. Alternatively, expression of a detectable transgene can be used for titer determination. Spin transduction is not mandatory, but it increases the titers obtained. Also, incubation at 32°C stabilizes retroviral particles and yields a better transduction efficiency.

References 1. Grosveld, F., van Assendelft, G. B., Greaves, D. R., and Kollias, G. (1987) Position-independent, high-level expression of the human beta-globin gene in transgenic mice. Cell 51, 975–985. 2. Buchman, A. R. and Berg, P. (1988) Comparison of intron-dependent and intronindependent gene expression. Mol. Cell. Biol. 8, 4395–4405. 3. Brinster, R. L., Allen, J. M., Behringer, R. R., Gelinas, R. E., and Palmiter, R. D. (1988) Introns increase transcriptional efficiency in transgenic mice. Proc. Natl. Acad. Sci. USA 85, 836–840. 4. Palmiter, R. D., Sandgren, E. P., Avarbock, M. R., Allen, D. D., and Brinster, R. L. (1991) Heterologous introns can enhance expression of transgenes in mice. Proc. Natl. Acad. Sc.i USA 88, 478–482. 5. Jonsson, J., Foresman, M., Wilson, N., and McIvor, R. (1992) Intron requirement for expression of the human purine nucleoside phosphorylase gene. Nucleic Acids Res. 20, 3191–3198. 6. Connelly, S., Gardner, J. M., McClelland, A., and Kaleko, M. (1996) High-level

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tissue-specific expression of functional human factor VIII in mice. Hum. Gene Ther. 7, 183–195. Jallat, S., Perraud, F., Dalemans, W., et al. (1990) Characterization of recombinant human factor IX expressed in transgenic mice and in derived trans-immortalized hepatic cell lines. EMBO J. 9, 3295–3301. Kurachi, S., Hitomi, Y., Furukawa, M., and Kurachi, K. (1995) Role of intron I in expression of the human factor IX gene, J. Biol. Chem. 270, 5276–5281. Wang, J. M., Zheng, H., Sugahara, Y., et al. (1996) Construction of human factor IX expression vectors in retroviral vector frames optimized for muscle-cells. Hum. Gene Ther. 7, 1743–1756. Nakai, H., Herzog, R. W., Hagstrom, J. N., et al. (1998) Adeno-associated viral vector-mediated gene transfer of human blood coagulation factor IX into mouse liver. Blood 91, 4600–4607. Sadelain, M., Wang, C., Antoniou, M., Grosveld, F., and Mulligan, R. (1995) Generation of a high-titer retroviral vector capable of expressing high levels of the human beta-globin gene. Proc. Natl. Acad. Sci. USA 92, 6728–6732. Jonsson, J. J., Habel, D. E., and McIvor, R. S. (1995) Retrovirus-mediated transduction of an engineered intron-containing purine nucleoside phosphorylase gene. Hum. Gene Ther. 6, 611–623. Strauss, J. H. and Strauss, E. G. (1994) The alphaviruses: gene expression, replication, and evolution. Microbiol. Rev. 58, 491–562. Wahlfors, J. J., Xanthopoulos, K. G., and Morgan, R. A. (1997) SemLiki Forest virus-mediated production of retroviral vector RNA in retroviral packaging cells. Hum. Gene Ther. 8, 2031–2041. Wahlfors, J. J. and Morgan, R. A. (1999) Production of minigene-containing retroviral vectors using an alphavirus/retrovirus hybrid vector system. Hum. Gene Ther. 10, 1197–1206. Miller, A. and Rosman, G. (1989) Improved retroviral vectors for gene transfer and expression. Biotechniques 7, 980–990. Berglund, P., Sjoberg, M., Garoff, H., Atkins, G., Sheahan, B., and Liljestrom, P. (1993) SemLiki Forest virus expression system: production of conditionally infectious recombinant particles. Biotechnology 11, 916–920. Nelson, D. M., Wahlfors, J. J., Chen, L., Onodera, M., and Morgan, R. A. (1998) Characterization of diverse viral vector preparations, using a simple and rapid whole-virion dot-blot method. Hum. Gene Ther. 9, 2401–2405. Li, K. J. and Garoff, H. (1996) Production of infectious recombinant moloney murine leukemia-virus particles in BHK cells using Semliki Forest virus-derived RNA expression vectors. Proc. Natl. Acad. Sci. USA 93, 11658–11663. Li, K. J. and Garoff H. (1998) Packaging of intron-containing genes into retrovirus vectors by alphavirus vectors, Proc. Natl. Acad. Sci. USA 95, 3650–3654.

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15 Retrovirus-Mediated Gene Transfer to Human Hematopoietic Stem Cells William P. Swaney, Enrico M. Novelli, Alfred B. Bahnson, and John A. Barranger

1. Introduction The ability of hematopoietic stem cells (HSCs) to engraft in a recipient and establish long-term repopulation of the hematopoietic system makes them ideal targets for gene therapy vectors designed to correct inherited or acquired diseases affecting the hematopoietic and immune systems. Monoclonal antibodies that bind to the CD34 antigen, a universally recognized marker for hematopoietic progenitor/stem cells (1–3), have been widely used to isolate HSCs from the hematopoietic tissues. Other cell surface antigens have also been targeted to subfractionate the heterogeneous CD34+ cells into subpopulations with distinct phenotypes and HSC potential (4). In vitro and in vivo functional assays have defined a hierarchy of biologically different cells, from subpopulations enriched for early long-term repopulating, retransplantable HSCs, to those only including committed progenitor cells. The colony-forming cell (CFC) assay provides an estimate of myeloerythroid progenitor cell potential (5); the assays for long-term culture initiating cells (LTCIC), blast colony-forming cells (CFC-blast), and cobblestone area-forming cells (CAFC) measure more primitive hematopoietic progenitors (6). On the other end of the spectrum, immunodeficient mouse models, such as the NOD/SCID assay, and other xenogeneic transplantation models like the preimmune fetal sheep allow measurement of the ability of cells to generate sustained, multilineage hematopoiesis after in vivo transplantation and therefore represent surrogate HSC assays (7). Animal assays are particularly valuable in gene therapy because they permit assessment of the efficiency of transduction and From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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persistence of expression of transferred genes in human hematopoietic cells in vivo. Of particular interest is the observation that transduced human CD34+ cells were able to repopulate the NOD/SCID strain (8–12), thereby providing a model for gene transfer studies in patients. Both in vitro (13,14) and in vivo assays (15,16) have indicated that the CD34+ subpopulation that is negative for the surface antigen CD38 is enriched for primitive HSCs. These studies have shown that the cells responsible for long-term, retransplantable hematopoiesis in NOD/SCID mice and fetal sheep reside in the CD34+ CD38– fraction. However, the definitive human HSC phenotype still remains elusive as additional putative markers for HSC such as AC133 (17,18) and KDR (19) are continuously discovered. Recent studies also demonstrate the presence in both primates and rodents of a rare CD34-Lin cell subset (20), which could be a more immature precursor of CD34+ cells and their subpopulations (21). It will be necessary to elucidate fully the functional characteristics and biologic behavior of these populations before targeted, highly efficient gene therapy strategies for human HSCs can be implemented consistently. A major impediment to retroviral transduction of HSCs has been their paucity in hematopoietic tissues. The CD34+ cells account for only 1–4% of mononuclear cells in the bone marrow (BM), 104. 7. The multiplicity of infection (MOI): TU/mL/n of cells to be infected for the following ranges: infection efficiency is primarily controlled by vector concentration (TU/mL), and MOI should be considered only for certain ranges of concentration of cells (>104 cells/mL) and vector (>106 TU/mL).

Acknowledgments The financial support of Telethon–Italy (grant A.143), MURST (grant 9905313431), and the EU (grant QLK3-1999-00859) is gratefully acknowledged. A.F. is the recipient of an AIDS program fellowship from ISS, Italy. References 1. Naldini, L. (1998) Lentiviruses as gene transfer agents for delivery to non-dividing cells Curr. Opin. Biotechnol. 9, 457–463. 2. Federico, M. (1999) Lentiviruses as gene delivery vectors Curr. Opin. Biotechnol. 10, 448–453. 3. Vigna, E. and Naldini, L. (2000) Lentiviral vectors: excellent tools for experimental gene transfer and promising candidates for gene therapy. J. Gene Med. 2, 308–316. 4. Trono, D. (2000) Lentiviral vectors: turning a deadly foe into a therapeutic agent. Gene Ther. 7, 20–23.

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5. Coffin, J., Hughes, S. H., and Varmus, H. E. (2000) Retroviruses. Cold Spring Harbor Laboratory Press,Cold Spring Harbor, NY.l 6. Frankel, A. D. and Young, J. A. (1998) HIV-1: fifteen proteins and an RNA. Annu. Rev. Biochem. 67, 1–25. 7. Emerman, M. and Malim, M. H. (1998) HIV-1 regulatory/accessory genes: keys to unraveling viral and host cell biology. Science 280, 1880–1884. 8. Wei, P., Garber, M. E., Fang, S. M., Fischer, W. H., and Jones, K. A. (1998) A novel CDK9-associated C-type cyclin interacts directly with HIV-1 Tat and mediates its high-affinity, loop-specific binding to TAR RNA. Cell 92, 451–462. 9. Bieniasz, P. D., Grdina, T. A., Bogerd, H. P., and Cullen, B. R. (1999) Recruitment of cyclin T1/P-TEFb to an HIV type 1 long terminal repeat promoter proximal RNA target is both necessary and sufficient for full activation of transcription. Proc. Natl. Acad. Sci. USA 96, 7791–7796. 10. Neville, M., Stutz, F., Lee, L., Davis, L. I., and Rosbash, M. (1997) The importinbeta family member Crm1p bridges the interaction between Rev and the nuclear pore complex during nuclear export. Curr. Biol. 7, 767–775. 11. Fornerod, M., Ohno, M., Yoshida, M., and Mattaj, I. W. (1997) CRM1 is an export receptor for leucine-rich nuclear export signals. Cell 90, 1051–1060. 12. Stade, K., Ford, C. S., Guthrie, C., and Weis, K. (1997) Exportin 1 (Crm1p) is an essential nuclear export factor. Cell 90, 1041–1050. 13. Pollard, V. W. and Malim, M. H. (1998) The HIV-1 Rev protein. Annu. Rev. Microbiol. 52, 491–532. 14. von Schwedler, U., Song, J., Aiken, C., and Trono, D. (1993) Vif is crucial for human immunodeficiency virus type 1 proviral DNA synthesis in infected cells. J. Virol. 67, 4945–4955. 15. Zhang, H., Pomerantz, R. J., Dornadula, G., and Sun, Y. (2000) Human immunodeficiency virus type 1 Vif protein is an integral component of an mRNP complex of viral RNA and could be involved in the viral RNA folding and packaging process. J. Virol. 74, 8252–8261. 16. Gottlinger, H. G., Dorfman, T., Cohen, E. A., and Haseltine, W. A. (1993) Vpu protein of human immunodeficiency virus type 1 enhances the release of capsids produced by gag gene constructs of widely divergent retroviruses. Proc. Natl. Acad. Sci. USA 90, 7381–7385. 17. Schubert, U., Anton, L. C., Bacik, I., et al. (1998) CD4 glycoprotein degradation induced by human immunodeficiency virus type 1 Vpu protein requires the function of proteasomes and the ubiquitin-conjugating pathway. J. Virol. 72, 2280–2288. 18. Garcia, J. V. and Miller, A. D. (1991) Serine phosphorylation-independent downregulation of cell-surface CD4 by nef. Nature 350, 508–511. 19. Miller, M. D., Warmerdam, M. T., Gaston, I., Greene, W. C., and Feinberg, M. B. (1994) The human immunodeficiency virus-1 nef gene product: a positive factor for viral infection and replication in primary lymphocytes and macrophages. J. Exp. Med. 179, 101–113. 20. Aiken, C. (1997) Pseudotyping human immunodeficiency virus type 1 (HIV-1) by the glycoprotein of vesicular stomatitis virus targets HIV-1 entry to an

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Minimal requirement for a lentivirus vector based on human immunodeficiency virus type 1. J. Virol. 72, 811–816. Mochizuki, H., Schwartz, J. P., Tanaka, K., Brady, R. O., and Reiser, J. (1998) High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells. J. Virol. 72, 8873–8883. Zufferey, R., Nagy, D., Mandel, R. J., Naldini, L., and Trono, D. (1997) Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nat. Biotechnol. 15, 871–875. Dull, T., Zufferey, R., Kelly, M., et al. (1998) A third-generation lentivirus vector with a conditional packaging system. J. Virol. 72, 8463–8471. Kafri, T., van Praag, H., Ouyang, L., Gage, F. H., and Verma, I. M. (1999) A packaging cell line for lentivirus vectors. J. Virol. 73, 576–584. Klages, N., Zufferey, R., and Trono, D. (2000) A stable system for the high-titer production of multiply attenuated lentiviral vectors. Mol. Ther. 2, 170–176. Parolin, C., Dorfman, T., Palu, G., Gottlinger, H., and Sodroski, J. (1994) Analysis in human immunodeficiency virus type 1 vectors of cis-acting sequences that affect gene transfer into human lymphocytes. J. Virol. 68, 3888–3895. Carroll, R., Lin, J. T., Dacquel, E. J., et al. (1994) A human immunodeficiency virus type 1 (HIV-1)-based retroviral vector system utilizing stable HIV-1 packaging cell lines. J. Virol. 68, 6047–6051. McBride, M. S., Schwartz, M. D., and Panganiban, A. T. (1997) Efficient encapsidation of human immunodeficiency virus type 1 vectors and further characterization of cis elements required for encapsidation. J. Virol. 71, 4544–4554. Berkowitz, R. D., Hammarskjold, M. L., Helga-Maria, C., Rekosh, D., and Goff, S. P. (1995) 5' Regions of HIV-1 RNAs are not sufficient for encapsidation: implications for the HIV-1 packaging signal. Virology 212, 718–723. Miyoshi, H., Blomer, U., Takahashi, M., Gage, F. H., and Verma, I. M. (1998) Development of a self-inactivating lentivirus vector. J. Virol. 72, 8150–8157. Zufferey, R., Dull, T., Mandel, R.J., et al. (1998) Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J. Virol. 72, 9873–9880. Iwakuma, T., Cui, Y., and Chang, L. J. (1999) Self-inactivating lentiviral vectors with U3 and U5 modifications. Virology 261, 120–132. Donello, J. E., Loeb, J. E., and Hope, T. J. (1998) Woodchuck hepatitis virus contains a tripartite posttranscriptional regulatory element. J. Virol. 72, 5085–5092. Deglon, N., Tseng, J. L., Bensadoun, J. C., et al. (2000) Self-inactivating lentiviral vectors with enhanced transgene expression as potential gene transfer system in Parkinson’s disease. Hum. Gene Ther. 11, 179–190. Zufferey, R., Donello, J. E., Trono, D., and Hope, T. J. (1999) Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J. Virol. 73, 2886–2892. Follenzi, A., Ailles, L. E., Bakovic, S., Geuna, M., and Naldini, L. (2000) Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nat. Genet. 25, 217–222.

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51. Zennou, V., Petit, C., Guetard, D., et al. (2000) HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 101, 173–185. 52. Charneau, P., Alizon, M., and Clavel, F. (1992) A second origin of DNA plusstrand synthesis is required for optimal human immunodeficiency virus replication. J. Virol. 66, 2814–2820. 53. Charneau, P., Mirambeau, G., Roux, P., et al. (1994) HIV-1 reverse transcription. A termination step at the center of the genome. J. Mol. Biol. 241, 651–662. 54. Ilyinskii, P. O. and Desrosiers, R. C. (1998) Identification of a sequence element immediately upstream of the polypurine tract that is essential for replication of simian immunodeficiency virus. EMBO J. 17, 3766–3774. 55. Blomer, U., Naldini, L., Kafri, T., et al. (1997) Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector. J. Virol. 71, 6641–6649. 56. May, C., Rivella, S., Callegari, J., et al. (2000) Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin. Nature 406, 82–86. 57. An, D. S., Wersto, R. P., Agricola, B. A., et al. (2000) Marking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cells. J. Virol. 74, 1286–1295. 58. Bukovsky, A. A., Song, J. P., and Naldini, L. (1999) Interaction of human immunodeficiency virus-derived vectors with wild-type virus in transduced cells. J. Virol. 73, 7087–7092. 59. Bonyhadi, M. L. and Kaneshima, H. (1997) The SCID-hu mouse: an in vivo model for HIV-1 infection in humans. Mol. Med. Today 3, 246–253. 60. DuBridge, R. B., Tang, P., Hsia, H. C., et al. (1987) Analysis of mutation in human cells by using an Epstein-Barr virus shuttle system. Mol. Cell Biol. 7, 379–387. 61. Graham, F. L., Smiley, J., Russell, W. C., and Nairn, R. (1977) Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J. Gen. Virol. 36, 59–74.

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20 Packaging Cell System for Lentivirus Vectors Preparation and Use Narasimhachar Srinivasakumar

1. Introduction Packaging systems based on human immunodeficiency virus type 1 (HIV1) can be used to transfer genes (both ex vivo and in vivo in experimental animals), with high efficiency into a wide variety of cell types including nondividing and terminally differentiated cells such as muscle and neuronal cells (1– 6). In this chapter, I begin with an overview of HIV-1 structure, genetics, and replication cycle, emphasizing those features essential for the creation of packaging systems based on HIV-1. Next, I describe the plasmid constructs for preparation of HIV-1 vector stocks, including some recent advances in the design of helper and gene transfer vectors. Finally, a detailed protocol for generation and testing of vectors is provided. Although HIV-1 is used as a prototype for other lentiviruses and there are many similarities between different viruses, there are also significant differences. The extensive knowledge base of HIV-1-based gene transfer systems can be readily adapted to develop gene transfer vectors based onother lentiviruses such as feline immunodeficiency virus (FIV; see Chapter 23). These other lentivirus vectors are likely to share many of the advantages of HIV-1 vectors. Because of space limitations, comparisons with other lentiviruses that highlight similarities or differences are not given. I recommend the excellent treatise on retroviruses (6a) edited by J.M. Coffin, S.H. Hughes, and H.E. Varmus (CSHL,1997) for this purpose and to support many of the statements made in this introduction.


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Fig. 1. Schematic representation of HIV-1 provirus (top) and a typical lentivirus packaging system consisting of a packaging plasmid, a gene transfer vector, and an envelope expression plasmid. Only relevant portions of the various constructs are shown. LTR, long terminal repeat; RRE, Rev responsive element.

1.1. HIV-1 Structure and Genetics The RNA genome of HIV-1 is about 9.7 kb in size. The reverse-transcribed and integrated form of the HIV-1 genome is called the provirus. The organization of the HIV-1 provirus is shown in Figure 1. Like other retroviruses, the provirus contains the long terminal repeat (LTR) elements at both the 5' and 3' ends of the provirus. Each LTR contains U3 (unique 3), R (repeat), and U5 (unique 5) regions. The U3 contains promoter and enhancer elements, and the R region contains the sequence for trans-acting response (TAR) element and signals for polyadenylation. The 5' end of U3 and the 3' end of U5 also contain sequences for recognition by the viral integrase protein to bring about recombination between the virus cDNA and the host chromosomal DNA. Between the two LTRs are coding regions for viral structural and regulatory proteins. Simple retroviruses have coding sequences for only three genes: gag, pol, and env. Complex retroviruses such as HIV contain coding sequences for at least


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six additional proteins: two regulatory proteins (Tat and Rev) and four accessory proteins (Vif, Vpr, Vpu, and Nef). Transcription begins at the first nucleotide of R in the 5' LTR and terminates at the last nucleotide of 3' R. Termination may not be very efficient and may proceed through to cellular flanking sequences. The various structural and regulatory proteins are synthesized from either full-length (Gag and Gag-Pol), partially spliced (e.g., Env and Vpu), or fully spliced messages (e.g., Tat, Rev, and Nef). 1.2. Virion Structural Proteins HIV-1, like other retroviruses, is an enveloped virus that contains two copies of a positive or message sense RNA genome within a cone-shaped core. Gag and Gag-Pol are polyproteins that contribute to most of the internal proteins of the virion. Upon proteolytic cleavage by the viral protease, the Gag polyprotein is split into the matrix (p17), capsid (p24), nucleocapsid (p7), and p6 protein. Upon cleavage, the Pol region of the Gag-Pol precursor yields protease, reverse transcriptase (RT), and integrase proteins (IN). The viral protease is released by autoproteolytic cleavage from the Gag-Pol precursor and then acts on the other cleavage sites in the Gag and Gag-Pol proteins. Except for the p17 or matrix protein that lines the inner aspect of the virus envelope, the other proteins conglomerate around the RNA genome to form the virion core. Vif, Vpr, and Nef are other proteins that are encapsulated in the virion. Although it was previously believed that Vif was packaged into virions by a nonspecific mechanism, recent evidence seems to indicate that Vif is incorporated into virions via its interaction with the genomic RNA (6b). The lipid envelope of the virion contains the transmembrane (TM) and surface (SU) glycoproteins gp41 and gp120, which are coded for in the env region. The SU glycoprotein is noncovalently attached to the TM protein and contains the binding sites for the CD4 receptor and the chemokine coreceptors such as CCR5 or CXCR4 depending on whether the virus is macrophage or T-cell tropic, respectively. The SU protein effects binding of the virion to target cells, whereas fusion of virion and target cell membrane is accomplished by the TM protein. The HIV-1 envelope glycoproteins can be replaced with envelope glycoproteins from other viruses such as Moloney murine leukemia virus (MMLV) or the vesicular stomatitis virus G (VSV-G) glycoprotein. This enables us to prepare virus stocks that can infect a wide variety of cells that do not bear either CD4 or the chemokine coreceptors. 1.3. Lentivirus Life Cycle Following binding of the virus particle to the cell surface receptor(s), fusion of virion and plasma membrane of the target cell ensues. This results in deposition of the capsid together with the RNA genome into the cytoplasm of the

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target cell. The reverse transcriptase then converts the genomic RNA into a double-stranded cDNA by a complicated procedure that involves the use of a cellular t-RNA primer that is packaged together with the genomic RNA in the virion and multiple jumps from one end of the molecule to the other. The reverse transcription process recreates a functional promoter at the 5' end of the provirus (6a). Following reverse transcription, the cDNA is transported through the nuclear pore into the nucleus. Recent studies have shown that during reverse transcription, a central DNA flap is created due to the presence of a central polypurine tract (cPPT) and central termination sequence (CTS) within the Pol coding sequence (7,8). The creation of this unique triple-stranded DNA region appears to be important for the nuclear import of preintegration complex (PIC), in both dividing and nondividing cells (7,9). Recent vector designs have, therefore, incorporated the cis signals (cPPT and CTS) for the creation of this central DNA flap and thereby allow more efficient nuclear import of vector genome. The viral matrix (p17), integrase, and Vpr proteins have also been implicated in the nuclear import of PICs in nondividing cells (10–14). Although both p17 and integrase have nuclear localization domains, there is some controversy regarding their roles in the nuclear import of PICs (15–17). Once the cDNA is imported, the viral integrase functions to insert the cDNA into the host-cell chromosome at a site that appears to be chosen in a random fashion. Upon activation of the infected cell, full-length messages are transcribed from the viral LTR that undergoes splicing to yield messages that code for synthesis of Tat, Rev, and Nef proteins. Tat and Rev enter the nucleus to increase gene expression from the viral LTR and effect nucleocytoplasmic transport of fulllength and partially spliced messages, respectively, as described below. The viral structural proteins, the full-length RNA genome, and the t-RNA primer come together at the plasma membrane of the cell decorated with the envelope glycoprotein to assemble into a virus particle. 1.4. HIV-1 Accessory and Regulatory Proteins 1.4.1. Tat The Tat protein is a transcriptional activator that enhances transcription from the viral LTR promoter and also increases the processivity of the RNA PolII transcription machinery, ensuring abundant amounts of full-length genomic message (18–20). The Tat protein achieves this by binding to the TAR element present at the 5' end of the newly synthesized RNA. Tat binds to a bulge in this stem loop of TAR and recruits cellular proteins to TAR (and thereby the viral LTR promoter). The host proteins recruited include the positive transcription elongation factor b (P-TEFb) and Tat-associated kinase complexes, which con-


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sist of, among other protein subunits, cyclin-T1 and the cyclin-dependent kinase CDK9. This complex phosphorylates the C-terminal domain of RNA polymerase II and increases its processivity. Tat has also been shown to recruit histone acetyltransferases (HAT) p300 and p300 CREB binding protein associated factor (p/CAF) to the viral promoter (21–23). The HAT proteins appear to be essential for optimal transcriptional activation of the viral promoter in the context of integrated vector but not in transient transfection assays. Tat is required in HIV-1-based packaging systems to ensure that adequate amounts of the gene transfer vector RNA are synthesized for encapsidation into the virus particles (24,25). Replacement of HIV enhancer and promoter elements within the U3 of the 5' LTR with elements from other promoters overcomes this requirement for Tat protein and allows one to create Tat-independent gene transfer vectors (see Subheading 1.6.2.3) (25,26). 1.4.2. Rev The Rev protein binds to a target sequence within the envelope coding region referred to as the Rev responsive element (RRE). Rev recruits the nuclear export factors Crm1 to RRE to bring about the transport of intron-containing messages (i.e., partially spliced and unspliced messages such as those coding for Gag and Pol proteins or the Env glycoprotein) into the cytoplasm (27–29). Without Rev, there is, therefore, no synthesis of these essential structural proteins, resulting in a nonreplicating virus. Thus, Rev is an attractive target for control of HIV-1 replication. Rev and RRE are required for expression of HIV1 subgenomic messages such as those used in the expression of viral Gag and Gag-Pol proteins in packaging or helper constructs (24,30). The RRE is also part of the gene transfer vector in most of the HIV-1 vector constructs reported to date. The RRE sequence is required to ensure efficient transport of the vector RNA into the cytoplasm in the presence of Rev, which allows encapsidation of the RNA into the assembling virion (24,31–33). 1.4.3. Nef The Nef protein is synthesized early after infection together with Tat and Rev and has pleiotropic effects. Nef has been shown to downmodulate cell surface expression of CD4 by inducing endocytosis, resulting in the degradation of this molecule in lysosomes (34–37). Since Nef is believed to an important contributor in the pathogenicity of AIDS by HIV (38), it may be prudent to remove this from HIV-based packaging systems in spite of its known positive effect on increasing the efficiency of reverse transcription during viral entry (39,40). Fortunately, this effect of Nef is restricted to certain types of envelope glycoproteins used for pseudotyping HIV vectors. For instance, Nef increases

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infectivity of virions pseudotyped with HIV-1 or amphotropic MMLV envelopes but not those pseudotyped with VSV-G (41,42). Nef can, therefore, be eliminated from packaging systems that employ VSV-G to pseudotype vectors. 1.4.4. Vpr Vpr is another protein with pleiotropic effects. It can cause cells to arrest in the G2 phase of the cell cycle (43–46). Cell-cycle arrest in G2 results in a modest increase in transcriptional output from the viral LTR promoter (46). Vpr has also been shown to be essential for importation of PIC into the nucleus of macrophages (14,47–49). Vpr is packaged into the virion at a ratio of one Vpr molecule to seven capsid protein (p24) monomers (50). Vpr is recruited into the virus particle through its interaction with the p6 region of the Gag molecule (51,52). When concentrated stocks of HIV-1 vector stocks are used in gene transfer experiments, Vpr delivered by the virus particles can result in apoptosis of target cells (53–55). So the advantages of using Vpr for nuclear import of PICs in some types of cells must be weighed against its propensity to cause apoptosis. 1.4.5. Vif and Vpu Vif has been shown to increase infectivity of virions produced in certain human T-cell lines (56,57). Vif appears to affect events after binding and fusion, during either uncoating or RT (58). Vpu has been shown to increase virion export in human cells but not in cell lines of simian origin (59). In spite of these known functions of Vif and Vpu, it appears that one can safely eliminate these proteins for preparation of high-titer virus stocks when using 293T cells (see below). 1.5. Constitutive Transport Element (CTE) Simpler retroviruses, such as the Mason-Pfizer monkey virus (MPMV), a type D retrovirus, utilize a structured RNA element that does not require the coexpression of a viral protein to achieve the transport of unspliced or introncontaining messages from the nucleus to the cytoplasm (60,61). These elements have been dubbed constitutive transport elements (CTEs). The CTE has been shown to substitute for Rev-RRE function not only in the context of the HIV-1 provirus (62,63) but also in subgenomic constructs used for the expression of viral helper proteins or gene transfer vector RNAs (24,32,33,64,65). In fact, packaging systems that completely lack Rev have been described (24,32), although these systems seem to perform a little less efficiently than the classical Rev-RRE system for production of lentivirus vector stocks. Further refinements in the use of these alternative transport elements from other viruses may


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Fig. 2. Schematic representation of packaging plasmids. The packaging plasmid regulated by MPMV-CTE/pA signal (bottom) also expresses a functional single-exon or 72-amino acid Tat protein (Tat72) (33). LTR, long terminal repeat; RRE, Rev responsive element; MPMV-CTE, Mason-Pfizer monkey virus/constitutive transport element.

allow enhanced titers and increased gene expression in transduced target cells. Rev-independent packaging systems may be useful for delivery of dominantnegative Rev genes into HIV-1 susceptible cells to effect a type of “intracellular immunization” against HIV-1 infection (65). 1.6. Lentivirus Packaging Systems A typical lentivirus packaging system (Fig. 1) consists of three components: 1) helper or packaging plasmids that encode for essential virus structural and regulatory proteins (with the exception of the envelope glycoprotein); 2) a plasmid that expresses an envelope glycoprotein from an unrelated virus such as the amphotropic MMLV or VSV-G glycoprotein; and 3) a gene transfer vector. 1.6.1. Packaging or Helper Constructs 1.6.1.1. FIRST GENERATION PACKAGING/HELPER PLASMID

Early versions of packaging plasmids (Fig. 2) encoded most viral structural and regulatory proteins with the exception of the envelope glycoprotein (5,66– 68). A deletion within the 5' untranslated region upstream of gag and within the encapsidation signal was engineered to reduce the efficiency of incorporation of the helper RNA and thereby prevent recombination between vector and helper RNA molecules. The viral LTR promoter was replaced with a heterologous promoter such as the cytomegalovirus immediate early promoter. The

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downstream or 3' LTR was replaced with a heterologous polyadenylation signal (e.g., from SV40 or the insulin gene or another gene). A deletion or mutation within Env ensured that no envelope glycoprotein was synthesized. The helper plasmid still expressed all other regulatory and accessory proteins of HIV-1. 1.6.1.2. SECOND-GENERATION PACKAGING PLASMID WITHOUT CODING REGIONS FOR VIF, VPR, OR VPU

More recent versions of packaging plasmids have further deletions and modifications to eliminate Vif, Vpr, and Vpu expression altogether (Fig. 2) or in various combinations (1,5,6,26,33). These helper constructs thus lack many of the accessory proteins that may be involved in HIV-1 pathogenicity and may render the packaging system safer. The goal of creating these minimal constructs is to design helper constructs that express only those genes that are essential for gene transfer into a wide variety of cells at high efficiency. 1.6.1.3. THIRD-GENERATION PACKAGING PLASMID USING SEGREGATION OF GAG/GAG-POL AND REV FUNCTIONS

For expression of the HIV-1 Gag and Gag-Pol proteins, normally one needs to insert the RRE downstream of the coding sequence and also express viral Rev protein, which allows the gag/pol message to be transported into the cytoplasm for translation. Early versions of the packaging plasmids contained the RRE and also expressed Rev. To further enhance safety, packaging systems have been devised in which the HIV-1 gag/pol and rev sequences have been segregated into separate plasmids (24,25). Tat has also been eliminated from this sytem by using Tat-independent gene transfer vectors (see Subheading 1.6.2.3.) Such a packaging system uses four plasmids for the creation of vector stocks instead of three. This increases the safety of the system by further decreasing the probability of recombination between the different helper plasmids and the gene transfer vector to recreate a replication-competent virus because multiple recombination steps need to occur to recreate a functional retrovirus. 1.6.1.4. RECENT MODIFICATIONS TO PACKAGING PLASMIDS

1.6.1.4.1. Segregation of Gag and Pol Coding Regions. A recent novel modification to the packaging system involves a clever approach toward separating Gag and Pol coding regions (69). The Gag-Protease proteins are expressed using one construct. The Pol proteins (RT and IN) are expressed as a Vpr-RT-IN fusion protein. The Vpr-RT-IN fusion protein is drawn into the assembling virus particle through the interaction between the Vpr and the p6


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Fig. 3. Schematic representation of a gene transfer vector based on HIV-1 and modifications to improve safety and expression (see text for details). LTR, long terminal repeat; RRE, Rev responsive element; CTE, constitutive transport element; CPPT/ CTS, central polypurine tract/central termination sequence; PIC, preintegration complex; SIN, self-inactivating; WPRE, woodchuck posttranslational regulatory element.

protein present in the C terminus of the Gag polyprotein. This approach appears to provide a higher margin of safety in lentivirus packaging system and considerably reduces the frequency of recombination between the packaging plasmids and the gene transfer vector. 1.6.1.4.2. Rev-Independent Packaging Plasmids. As alluded to earlier, the dependence of gag/pol expression on RRE and Rev can be eliminated by using CTEs from other viruses (Fig. 2) (24,26,32,33,64,65,68). Studies have indicated that CTEs function better if they are positioned toward the 3' end of the expression cassette (70,71). Also, one recent study showed that multiple copies of CTE may be better than single copies of the element for obtaining high levels of gag/pol expression (70). Such constructs showed gene expression levels exceeding those based on Rev and RRE. 1.6.2. Gene Transfer Vectors The ideal gene transfer vector will lack all viral protein coding sequences and have a capacity for large transgenes. It should possess, in addition to the transgene expression cassette, all cis-acting sequences for efficient packaging, nucleocytoplasmic transport, reverse transcription, and integration of the vector RNA. It is believed that HIV-1 vectors can deliver a transgene expression cassette of approximately 8–11 kb in length.

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1.6.2.1. FIRST-GENERATION GENE TRANSFER VECTORS

The first-generation vectors (Fig. 3) carried a deletion between the middle of the gag coding region and well into the env coding region, thereby essentially eliminating all viral coding regions (67). It may not be possible to eliminate gag sequences completely because the sequence at the beginning of the gag has been shown to contain elements that can increase packaging efficiency of the vector RNA (72–77). A frame shift mutation or stop codon inserted within the gag reading frame can ensure premature termination of translation. The vectors also contain the RRE between the major 5' splice donor site and the 3' tat/rev splice acceptor site. The transgene expression cassette is usually positioned between the BamHI site within the second coding exon of rev and the XhoI site within nef, effectively shutting out Nef expression. Polyadenylation of the RNA (including that derived from the internal promoter) occurs using signals present in the 3'U3 and R sequences within the LTR. The most common internal promoter enhancer elements used in HIV-1 vectors are those derived from the cytomegalovirus immediate early gene and the cellular phosphoglycerokinase promoter from mouse or human. It is believed that one may be able to replace these promoters with other tissue-specific or regulatable ones. 1.6.2.2. REV-INDEPENDENT HIV-1 VECTORS

The requirement of Rev for expression of vector RNA containing RRE can be eliminated by using the CTE downstream of the transgene expression cassette (Fig. 3) (24,32,33,64). Vectors containing the CTE can be used to create a Rev-independent packaging system for delivery of transdominant negative Rev (65). 1.6.2.3. TAT-INDEPENDENT HIV-1 VECTORS

The first-generation HIV-1 vectors required Tat to obtain optimal titers, since expression from the viral LTR promoter requires coexpression of Tat. To overcome this, hybrid promoters that use enhancer elements from other viruses, instead of those present in the U3 of HIV-1, have been created (Fig. 3) (25,26). These vectors appear to be nearly as efficient in terms of vector titer as the original Tat-dependent vectors that contained the wild type HIV-1 LTR. Although there is a report showing that Tat, in addition to its effect on transcription from the viral LTR, can also effect the efficiency of reverse transcription (78), studies using HIV-1 vectors have not revealed this requirement (25,26,33). 1.6.2.4. MODIFICATIONS TO VECTOR TO IMPROVE SAFETY AND EFFICACY

Figure 3 shows various modifications to lentivirus vectors to improve efficacy and safety.


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1.6.2.4.1. Self-Inactivating HIV-1 Vectors. It has been shown that most of the U3 region of the 3' LTR can be safely deleted without compromising vector titer (79,80). Such a deletion ensures that transcription from the 5' LTR promoter is efficiently suppressed following reverse transcription and integration into the target cell chromosome. Another advantage of using vectors with deletions in the U3 region is the enhanced transgene expression noted from the internal promoters in such vectors (79). This is probably because of a decrease in promoter competition between the viral LTR and the internal promoter. 1.6.2.4.2. Addition of Posttranscriptional Regulatory Elements from Woodchuck Hepatitis Virus. Hepatitis B viruses contain cis-acting elements that can substitute for Rev and RRE function in HIV-1 subgenomic constructs (81–83). Experiments have revealed that addition of a 600 bp posttranscriptional regulatory element from woodchuck hepatitis virus (WPRE) in retroviral and lentiviral vectors downstream of the transgene can increase expression by five to eightfold (Fig. 3) (84). 1.6.2.4.3. Addition of cPPT and CTS. Recent studies have demonstrated that a central DNA flap created during reverse transcription of lentivirus RNA is important in the nuclear importation of PICs (7,9) (see Subheading 1.3.). The cis-acting sequences required for the creation of this central DNA flap, the cPPT and CTS, within the pol coding region, are being increasingly utilized in lentivirus vectors to improve virus titer in both dividing and nondividing cells. 1.6.3. Envelope Glycoproteins Used for Pseudotyping Lentivirus Vectors The most popular envelope glycoprotein that has been used for pseudotyping lentivirus vectors is the VSV-G glycoprotein, which is quite stable under high centrifugation forces. This allows vectors pseudotyped with VSV-G to be readily concentrated by ultracentrifugation. In contrast to VSV-G, the amphotropic MMLV envelope pseudotyped vectors cannot be concentrated by ultracentrifugation without loss of titer. To concentrate vectors pseudotyped with amphotropic envelope, one has to use alternative methods based on ultrafiltration using molecular weight cutoff filters (further described under Subheading 3.2.2.). 1.7. Packaging Systems Depending on the RNA transport element being used, one can design three types of packaging systems for production of HIV-1 vector stocks (Table 1) (33). The traditional or classical HIV-1 packaging system uses RRE and Rev for the expression of both helper and gene transfer vector RNAs. The second packaging system uses MPMV-CTE for expression of helper and gene transfer vector RNAs. The third type, called the combination or reciprocal packaging

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Table 1 Classification of Packaging Systems Based on RNA Transport Elements Used for Expression of Helper and Gene Transfer Vector RNAsa RNA transport element in Packaging system RRE/Rev CTE Reciprocal-1 Reciprocal-2 a RRE,

Helper plasmid

Gene transfer vector

Rev requirement

RRE CTE CTE RRE

RRE CTE RRE CTE

Yes No Yes Yes

Rev responsive element; CTE, constitutive transport element.

system, utilizes Rev/RRE for expression of one component of the packaging system and CTE for the other component (33,64). There are two regions of homology between the helper and gene transfer vector constructs. One is at the 5' end of the gag coding region, and the other is the shared RRE or CTE toward the 3' end of the helper construct and the same element present within the gene transfer vector. Using dissimilar transport elements at the 3' end of the helper plasmid and the gene transfer vector in the combination packaging system may render the system safer by reducing the chance of replication-competent retrovirus (RCR) formation due to a recombination event. Taking this idea further, several investigators have resorted to decreasing the homology at the gag end of the helper and gene transfer vector constructs. One approach has been to “humanize” gag codons systematically in the helper plasmid (85). This not only reduces the homology in the gag region, it also renders gag expression Rev independent. Elimination of homology at the gag end and at the 3' end by removal of RRE in the helper plasmid makes this packaging system one of the safest described to date. An alternate approach to the same goal has been to use a helper construct derived from simian immunodeficiency virus (SIV) (86) based on the observation that SIV can cross-package HIV-1 RNA (87). However such packaging systems are still in their infancy and need to be developed further. 1.8. Advantages and Disadvantages for Lentivirus Vectors Because of their ability to integrate into the host chromosome, lentivirus vectors, like oncoretroviral vectors and unlike many other gene transfer vectors, can transduce cells permanently. Thus they have the capability to effect long-term gene expression. Lentiviruses also have the advantage that they can transduce terminally differentiated and growth-arrested cells efficiently.


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Oncoretroviral vectors, on the other hand, can only transduce growing cells (88–90). Because of the random nature of integration, lentiviruses have some of the same disadvantages as other retroviruses, such as the possibility of either inactivating cellular genes (e.g., tumor suppressor genes) or activating or causing overexpression of other genes (e.g., oncogenes). Inadvertent activation of cellular genes, including oncogenes, can be avoided by using later generations of self-inactivating vectors, which are devoid of promoter and enhancer elements in the viral 3' LTR (see above). It may be possible to overcome the drawback of random integration by redirecting PICs to specific regions of the host chromosome by fusing sequence-specific DNA binding domains to the viral integrase (91,92). Most investigators currently use a transient transfection approach to produce vector stocks. A drawback of this procedure is that there may be a significant degree of rearrangement of the input DNAs. This can lead to contamination of vector stocks with defective vector genomes. To produce “clean” vector stocks, it may be preferable to derive well-characterized packaging cell lines. The major hurdle for the creation of packaging cell lines appears to be the toxicity of certain viral proteins. For instance, Vpr causes cells to arrest in the G2 phase of the cell cycle (43–45) and therefore would not be conducive for producing cell lines that express high levels of this protein. Likewise, the viral protease has been shown to also cleave cellular proteins, which could interfere with the establishment of cell lines that stably express viral Gag-Pol proteins (93,94). VSV-G protein expression is also toxic to cells. Although cell lines that constitutively express viral packaging proteins have been described (24,95,96), more recent approaches toward the creation of lentivirus packaging cell lines resort to the use of inducible or regulatable promoters to overcome potential toxic effects of viral proteins (66,97). The construction of packaging cell lines using regulated promoters is beyond the scope of this chapter and the interested reader is referred to recent articles (66,97) describing such cell lines. 2. Materials 2.1. Cell Culture 1. Adenovirus transformed human embryonic kidney cell line expressing SV40 Tantigen (293T cells). 293T cells can be obtained from American Type Culture Collection (Rockville, MD; ATCC cat. no. SD-3515). 2. Phosphate-buffered saline (PBS) without divalent cations. 3. Growth medium (DMEM/10% fetal bovine serum [FBS]). Dulbecco’s modified Eagle’s medium (DMEM) with 2 mm L-glutamine, 100 U/mL penicillin, 100 μg/ mL streptomycin, and 10% heat-inactivated FBS (see Note 1). 4. Tissue culture flasks: 25 cm2 or larger.

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2.2. Calcium Phosphate-Mediated Transfection 1. Plasmid constructs: Production of vector stocks requires cotransfection of three or more plasmids, one or more packaging plasmids that provide helper function, a gene transfer vector, and an envelope glycoprotein-expressing plasmid. Various types of packaging constructs, gene transfer vectors and envelope expression constructs have been described above (see Note 2). 2. HEPES-buffered saline (HeBS), 2× (50 mM HEPES, 10 mM KCl, 12 mM dextrose, 280 mM NaCl, 1.5 mM Na2HPO4, pH 7.05). To make 500 mL of stock buffer, add 5.96 g HEPES, 0.37 g KCl, 1.08 g dextrose, 8.18 g NaCl, and 5 mL 150 mM Na2HPO4•7H2O (20 g/500 mL of deionized distilled water). It is prudent to make several lots, adjusted to pH 7.05, since even slight differences in pH can have a dramatic effect on transfection efficiency. Filter through a 0.2-μM filter and store in aliquots at –20°C. Test aliquots from each lot for transfection efficiency using a green fluorescent protein (GFP) reporter plasmid. Keep the lot that gives the highest transfection efficiency. Before use, warm to room temperature and vortex to achieve uniform mixing. Prepare fresh lots every 6–12 months (see Note 3). 3. 2.5 M calcium chloride (CaCl2). Store in aliquots at –20°C. Before use, warm to room temperature and vortex to achieve uniform mixing.

2.3. Concentration of Virus Stock 1. Ultracentrifuge tubes (Beckman). Place inverted in racks, wrap with aluminum foil, and autoclave at 120°C for 15 min. 2. Appropriate rotors and an ultracentrifuge. 3. Centrifugal ultrafiltration devices. 100,000-kDa molecular weight cutoff filters (e.g., Centricon Plus-20 or Centricon Plus-80 from Millipore or Macrosep centrifugal concentrators from Pall Gelman). 4. High-speed centrifuge.

2.4. Titration of Virus Stock 1. 2. 3. 4.

6-well tissue culture plates. PBS with calcium and magnesium. Cell culture medium appropriate for cell line being used. Polybrene (hexadimethrine bromide) or DEAE-dextran. Make 1 mg/mL stock in PBS. Filter using 0.45-μm filter and store at 4°C. 5. 4% paraformaldehyde. Add 4 g of paraformaldehyde to 85 mL of water. Warm to 60°C in a water bath. Add a few drops of 2 M NaOH. Return to water bath and mix contents every few minutes. When paraformaldehyde is completely dissolved, add 10 mL of 10× PBS. Adjust pH to 7.4–7.6. Filter through a 0.45 μm filter and store at 4°C. Use within 1 week of preparation.

2.5. Detection of Replication-Competent Retrovirus (RCR) 1. Materials for phlebotomy (tourniquet, sterile syringe with appropriate size needle, sterile gauze).


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2. Heparin-containing tube (0.2 mL of 1000 U/mL) for collection of peripheral blood. 3. Histopaque. 4. Phytohemagglutinin (PHA; Sigma, cat. no. L8902). 5. Interleukin-2 (IL-2) (T-cell growth factor [TCGF]). 6. RPMI-10: RPMI-1640 with 10% heat-inactivated FBS, 100 U/mL penicillin, 100 μg/mL streptomycin, 0.05 μM 2-mercaptoethanol (2-ME). 7. HIV-p24 antigen detection kit (NEN-Dupont or Zeptometrix or other manufacturer).

3. Methods 3.1. Generation of Virus Stocks by Calcium Phosphate–Mediated Transient Transfection Method 293T cells can be transfected to high efficiency and are preferred for production of virus stocks by the calcium phosphate-mediated transient transfection method. The production of virus stocks requires the transfection of a helper plasmid(or plasmids) that expresses Gag, Gag-Pol, Tat, and Rev, a gene transfer vector encoding the transgene expression cassette, and an envelope glycoprotein expressing plasmid. Tat is required for expression of full-length gene transfer vector RNA, whereas Rev is required for the transport of this message into the cytoplasm for encapsidation by the Gag and Gag-Pol proteins into the virus particle. Packaging systems that do not require Tat or Rev protein for production of vector stocks have been described (see Subheading 1.6.1.3.) but are not in widespread use. It is important to use clean plasmid DNA for transfections (see Note 2). It is imperative that appropriate biosafety practices should be used while generating and using lentivirus vector stocks (see Note 3) 1. Seed 2.5 × 106 293T cells in each T25 flask in 4 mL of medium 1 day before transfection. This usually gives 60–80% confluency in 24 h. 2. The next day, make up DNAs in 450 μL of water in a sterile microcentrifuge tube (2-mL capacity). I typically use 3.75 μg of packaging plasmid, 0.2 μg of VSV-Gexpressing plasmid, and 7.5 μg of gene transfer vector for transfection of cells in a T25 flask. Add 50 μL of 2.5 M CaCl2. Mix well and add 500 μL of 2× HeBS, in drops, while bubbling air through the DNA/CaCl2 mix. Bubbling can be carried out using a 1-mL sterile, cotton-plugged disposable plastic serologic pipet with the help of a pipet-aid. An EDP-Plus electronic pipet (Rainin) set in the “titrate” mode allows one to add the HeBS dropwise consistently between different samples. The procedure can be scaled up for larger size flasks (see Note 5). The amount of different DNAs to be used for transfection depends on many factors (see Note 6). 3. Add the DNA/CaCl2 solution to the cells within 1–2 min of preparation. 4. Abundant fine granular precipitate is usually visible the next morning, both in the medium and around the cells. Replace with 4 mL fresh medium next morning.

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Addition of chloroquine diphosphate or sodium butyrate can increase yields (see Note 7). 5. Harvest the medium at approx 60–72 h post-transfection by centrifugation at 1400g for 15 min at 4°C or by filtration through a 0.45-μm filter. One can get more mileage out of each transfection by harvesting and replacing medium every day for 3–4 days (see Note 8).

3.2. Concentration of Virus The transient transfection method generally yields titers in the range of 105– infectious units/mL. To obtain higher titers, one can concentrate the viruscontaining supernatant either by ultracentrifugation or by ultrafiltration using molecular weight cutoff centrifugation filters. Vectors pseudotyped with most envelope glycoproteins can be concentrated using ultrafiltration but this method suffers from some drawbacks (see Note 9). Ultracentrifugation is the usual method for concentration of VSV-G pseudotyped vectors. 106

3.2.1. Ultracentrifugation Method 1. Clarify virus-containing supernatant from transfected cell cultures by either centrifugation at 1400g for 15 min at 4°C or by filtration through a 0.45-μM filter. 2. Centrifuge at 100,000g for 2 h at 4°C using an SW-41 or SW28 (Beckman) rotor depending on the volume of supernatant being concentrated. 3. Carefully aspirate the supernatant and add 1/50th to 1/100th vol of DMEM/10% FBS. Vortex for 15–20 s and keep on ice. Repeat vortexing 3 or 4 times an hour for about 2 h. 4. Aliquot in 5–50-μL amounts and freeze at –80°C.

3.2.2. Concentration by Ultrafiltration Using Centrifugal Concentration Devices See Note 9. 1. Clear supernatant to be concentrated by filtration through 0.45-μm filters or by centrifugation at 1,400g for 15 min at 4°C. 2. Add cleared supernatant to the centrifugation filter devices with 100-KDa molecular weight cutoff filters. 3. Spin at the manufacturer’s recommended speed for a duration that yields the desired concentration. 4. Recover sample by simple decantation or by a reverse-spin procedure. 5. Aliquot and freeze down at –80°C.

3.3. Titration of Vectors Titration to detect the number of infectious units/mL in the virus stock consists of testing serial dilutions of the stock on appropriate target cells. The


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method and time it takes to determine the titer depends on the particular marker gene encoded in the gene transfer vector. For example, vectors with GFP or luciferase marker can be harvested about 2–3 days postinfection. For vectors with drug-resistant markers (e.g., hygromycin phosphotransferase or neomycin phosphotransferase genes, it takes approximately 2 weeks for the drugresistant colonies to form. 1. Subculture cells to be infected (target cells) into 6-well plates. Seed 2 × 105 cells/ well 1 day prior to virus infection. 2. Make dilutions of virus stock in cell culture medium containing DEAE-dextran or Polybrene (8 μg/mL). 3. Rinse wells twice with PBS containing calcium and magnesium to remove any floating cells. 4. Add 1 mL of virus dilution from step 2 to each well. Alternatively, if testing only small amounts of virus stock (e.g., from concentrates), add virus directly to well containing 1 mL of medium with an appropriate amount of DEAE-dextran or Polybrene. 4. Incubate plates at 37°C and 5% CO2. 5. Next morning add 2 mL of complete medium to each well and continue incubation at 37°C and 5% CO2 depending on the marker gene present in the vector. 6. For vectors encoding drug resistance markers (e.g., hygromycin or neomycin phosphotransferase genes), start selection 48 h postinfection by replacing medium with medium containing selection agent. Replace medium every 3–4 days with fresh medium containing selection agent. 8. Fix cells after 12–14 days with 0.5% crystal violet in 50% methanol when no live or adherent cells are seen in control (uninfected) wells and colonies are of sufficient size in test wells. 9. Enumerate colonies and estimate titer from amount or dilution used for infection.

3.3.1. Fixing Cells for GFP-Encoding Vectors For GFP-encoding vectors, cells are typically harvested 48–72 h post-infection. Titer determination using GFP reporter may be complicated by pseudotransduction (see Note 10). 1. 2. 3. 4. 5. 6.

Rinse wells twice with PBS without calcium and magnesium (2 mL/wash). Add 0.3 mL trypsin to each well. Incubate for 5 min at 37°C. Neutralize trypsin by adding 2 mL cell culture medium with serum. Pipet up and down to break up clumps and transfer cells to a 15-mL conical tube. Wash out wells with additional 2 mL of medium or PBS and add to previous harvest in the 15-mL tube. 7. Spin down cells at 200g at 4°C. 8. Wash cells once with 4 mL of PBS.

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9. Remove PBS and dislodge the cells by tapping the tube or running the tube on top of a test tube rack. 10. Add 0.5–1 mL PBS with 4% paraformaldehyde (freshly prepared) dropwise while vortexing gently. 11. Estimate percent positive for GFP by flow cytometry. GFP released from transduced can adsorb nonspecifically onto the surface of nontransduced cells. However, the two populations can be usually distinguished by FACS analysis.

3.4. Assays for Replication Competent Retrovirus (RCR) For obvious reasons, the chance of recreating a replication-competent HIV is impossible when using heterologous envelope constructs during transfection of 293T cells. There is, however, a possibility of formation of a novel RCR as a result of recombination among packaging plasmid, gene transfer vector, and a heterologous envelope-expressing construct. To detect RCR capable of growing in human peripheral blood mononuclear cells (PBMCs), an aliquot of concentrated virus stocks is used for infection of PBMCs (see Subheading 3.4.1.). The transduced cells are maintained in culture for at least 2 weeks and periodically monitored for the release of HIV-1 p24 in the culture supernatant. 3.4.1. Infection of PBMCs 1. Draw 15 mL of blood into a syringe containing 0.2 mL of heparin (1000 U/mL). Dilute to 30 mL with PBS. 2. Layer on 7.5 mL of Histopaque. 3. Centrifuge at 500g for 30 min at room temperature. 4. Remove top portion carefully with a 25-mL pipet. 5. Remove interphase containing PBMCs with a pipet and transfer to a new tube. 6. Dilute with 15 mL of PBS. 7. Spin down cells at 500g for 5 min. 8. Resuspend cells in 50 mL of PBS. 9. Spin cells down once again. 10. Repeat washes 2 more times (3 washes total). Count cells before final wash. 11. Resuspend cells to a concentration of 2 × 106 cells/mL in RPMI-10 with 0.05 μM 2-ME and and 2 μg of PHA/mL. 12. Incubate flask at 37°C, 5%CO2 for 48 h. 13. Spin down all mononuclear cells from flask at 550g for 5 min. 14. Resuspend in RMPI-10 to give 4 × 106 cells/mL. 15. Distribute 0.5 mL of cell suspension in each well of a 24-well plate. 16. Add an aliquot of concentrated virus stock to each well. 17. Add Polybrene in PBS to each well to give 8 μg/mL final concentration. 18. Incubate cells at 37°C, 5% CO2. 19. Next day, transfer mock and HIV-infected cultures to 15-mL screw-capped centrifuge tubes. 20. Spin down cells at 500g for 5 min.

Packaging Cell System for Lentivirus Vectors 21. 22. 23. 24.

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Save supernatant for analysis of p24. Resuspend cells in RPMI-10 with 5% IL-2 and return to original wells. Repeat this procedure twice weekly for 14 days. Test all saved supernatants for HIV-1 p24 antigen using a commercial kit per the manufacturer’s instructions.

3.4.2. Marker Rescue/Marker Mobilization Assay Gene transfer by retrovirus vectors to target cells is expected to be confined to one replicative cycle. That is, the supernatant from transduced cells should not contain vectors that can transfer the marker into naïve target cells—unless the initial stock used for production of virus stock contains RCR. The marker rescue/mobilization assays are devised to detect such RCRs. One can increase the sensitivity of detection of RCRs by using target cells that already harbor a vector that encodes a drug resistance marker. 1. Infect HeLa or other indicator cells with an aliquot of virus stock (approximately 10% of the volume used in the gene transfer experiment may be a suitable volume for detection of RCR). 2. The next day split the cells at a ratio of 1:50. Add Polybrene to 2 μg/mL in the medium to aid the spread of any RCR that may be present. 3. After 3–4 days, when 50% confluent, change to medium without Polybrene. 4. The following day harvest supernatant and clear by filtration through a 0.45-μm filter or by centrifugation at 1400g at 4°C for 15 min. 5. Concentrate the supernatant by using molecular weight cutoff filters or by ultracentrifugation (see Subheading 3.2.1.). 6. Infect fresh cells with unconcentrated and concentrated supernatant and assay for marker (either by starting drug selection or by assaying otherwise for the marker).

3.4.3. Assays for Partial Recombinants The first step toward the creation of RCR probably involves a recombination event between the packaging plasmid and the gene transfer vector. Such a recombinant may be able to produce either Gag protein or one of the accessory or regulatory proteins such as Tat. A recombinant vector that contains a Tat coding sequence can be detected using cell lines that encode the β-galactosidase gene under control of the HIV-1 LTR (see Note 11). Gag production can be monitored by assaying supernatants of transduced cell cultures for HIV-1 p24 using commercial kits. 4. Notes 1. Maintain 293T cells in DMEM/10% FBS. Split cells at a ratio of approximately 1:10 or 1:20 every 3–4 days. For a T225 flask, seeding at 2.5 × 106 cells should yield a near confluent monolayer in about 4 days. The cells should not be allowed

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4.

5.

6.

7.

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to overgrow. The cells are very sensitive to drying and readily detach from the surface even during rinsing procedures prior to trypsinization. Freeze down cells when in a low passage number in growth medium containing 10% dimethyl sulfoxide at a concentration of 5 × 106 cells per vial. After about 20 passages, recover fresh cells from the frozen stock. Plasmids used for transfection should be very clean. I use Qiagen columns for preparation of DNAs for transfection. Make fresh 2× HeBS every 6–12 months and freeze in aliquots. If no precipitate is seen the day following the transfection, it is likely that the pH is not optimal. Make a fresh batch of buffer. The easiest way to determine transfection efficiency is by using a GFP-expressing reporter plasmid. Transfection efficiency should be >50% as judged by fluorescence microscopy. Biosafety concerns. It is highly recommended that Centers for Disease Control (CDC)/National Institutes for Health (NIH) and institutional biosafety guidelines be followed for preparation and use of retroviral and lentivirus vectors. I currently use near BSL-3 practices in a BSL-2 laboratory. This involves, among other required safety practices, the disinfection of all materials that come in contact with virus with 10% bleach (made fresh daily) inside the biologic safety cabinet and bagging the potentially contaminated materials within the cabinet before bringing the material out for autoclaving and disposal. Details of how to set up a BSL-2 and BSL–3 laboratory should be available with your Institutional Biosafety Committee and are also available from the CDC and NIH (HHS Publication No. [CDC] 93-8395). I have successfully scaled up the protocol for transfection in T225 flasks without a diminution of virus yield. For these larger volumes of DNA/CaCl2 and HeBS solutions, use appropriately larger size tubes for making the calcium phosphateDNA precipitates (e.g., 50-mL sterile screw-capped tubes). The amount of various constructs to be used for transfection will obviously depend on expression levels obtained from each construct. This will vary from one construct to another depending on vector backbone and promoter/enhancer elements. Thus, for any new construct, the optimal amount to be used for transfection must be determined by a titration experiment to vary the different DNAs systematically. Modest increases in virus yields can be achieved by using chloroquine diphosphate and/or sodium butyrate. For treatment with chloroquine, prior to transfection, remove medium and gently add fresh growth medium containing 25 μM of chloroquine. Replace medium after 10 h (7–12 h). For treatment with sodium butyrate, replace medium 1 day after transfection (approx 10 h later) with medium containing 10 mM sodium butyrate. Leave it on for 12 h and then change to medium without sodium butyrate. These modifications, either adding sodium butyrate alone or both chloroquine and sodium butyrate in the medium, in our hands, yielded about a twofold increase in virus titer. Virus-containing supernatant can be harvested daily for 3 or 4 days starting 24 h after the first medium change. Clear each harvest by centrifugation or filtration through 0.45-μM filters and store on ice in a covered Styrofoam container at 4°C


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until all the harvests have accumulated. The virus in the pooled supernatant can be concentrated by ultracentrifugation or by ultrafiltration. 9. Concentration of virus particles using molecular weight cutoff filters frequently concentrates inhibitors that reduce the titer of the preparation. The inhibitors are believed to consist of sulfated proteoglycans (98,99). Attempts have been made to remove these inhibitors using enzymes such as chondroitinase ABC, resulting in modest improvements in titer (98,100). 10. Pseudotransduction is a type of protein or DNA delivery in the absence of bona fide infection (101–103). The marker protein or plasmid DNA is incorporated into the virion. Upon binding and fusion of the virus particles with target cell plasma membrane, the protein or DNA is then delivered to the cytoplasm. If sufficient quantity of protein or DNA is delivered, one may wrongly conclude that the target cells were expressing the protein as a result of authentic retrovirus infection process. Pseudotransduction has been observed with highly concentrated preparations of VSV-G pseudotyped vectors. To distinguish between authentic and pseudotransduction, one can use azidothymidine (AZT), an inhibitor of HIV-1 RT (32). The treatment of target cells with AZT (10 μM/mL) will allow the virus particles to bind and fuse with the plasma membrane but should interfere with the reverse transcription of incoming virus RNA and thereby abort the infection process. Under these circumstances, pseudotransduction by protein or DNA delivery is still possible, but no true transduction can occur. As an alternative approach, investigators have used packaging plasmids that have a mutation in the viral integrase (102) to prevent integration of the reverse-transcribed genome into the host chromosome. In this situation, the GFP detected in the target cells may be attributable to transcription from unintegrated vector genome and not necessarily all from protein delivery. It has been observed that expression of GFP caused by pseudotransduction gradually decreases with time and is negligible after 5 days post infection. Thus it may be prudent to measure or enumerate GFP-expressing cells in the target cell population 5 or more days after infection. 11. To detect partial recombinants that express Tat, many investigators have used target cells containing the ß-galactosidase reporter gene under control of the HIV1 LTR. HeLa-CD4-LTR-ß-Gal and MAGI-CCR5 are two such cell lines available from the NIH-AIDS Research and Reference Reagent Program. A detailed protocol for staining cells for detection of ß-galactosidase expression is provided with the cell lines.

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21 Lentiviral Vectors Preparation and Use Lung-Ji Chang and Anne-Kathrin Zaiss

1. Introduction Lentiviruses, such as human immunodeficiency virus (HIV), feline immunodeficiency virus (FIV), and equine infectious anemia virus (EIAV), are members of the Retroviridae, viruses with enveloped capsids and a plus-stranded RNA genome. Like all retroviruses, the RNA genome of lentivirus is converted to DNA by reverse transcription after infection and is subsequently stably integrated into the host cell genome. However, unlike other retroviruses, which mainly infect dividing cells, lentiviruses can infect both dividing and nondividing cells (1–3). Gene therapy viral vectors are produced by cotransfection of plasmids encoding viral envelopes, capsids, enzymes, and viral RNA. The specific tissue tropism of the lentiviral envelope restricts its use as a gene transfer vector. This limitation has been overcome by pseudotyping the viral envelope with vesicular stomatitis virus G (VSV-G) glycoprotein (4,5). The aim of this chapter is to describe the general procedures developed for the preparation and use of an HIV type 1 (HIV-1)-based lentiviral vector system. Detailed descriptions of lentiviral molecular biology can be found in several recent reviews (1,6,7). 1.1. Lentiviral Genome Structure and Vector Elements Lentiviruses are classified as complex retroviruses because of the multiple regulatory steps involved in their life cycle. The lentivirus genome is a diploid, plus-stranded RNA that is reverse transcribed into DNA (called provirus) and From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Genomic structure of HIV-1. Organization of HIV-1 genes and essential genetic elements in the proviral DNA and viral RNA. The transcription of viral RNA starts from the 5' terminus of R. Viral proteins except for Gag-Pol are expressed from alternatively spliced viral RNAs using a list of 5' and 3' splice junctions (s.j.) as depicted by solid arrowheads.

integrated in the host cell chromosomes (Fig. 1). The proviral genome is comprised of three conserved genes termed gag (group-specific antigen), pol (polymerase, reverse transcriptase), and env (envelope), which are flanked by elements called long terminal repeats (LTRs). LTRs contain the left and right integration attachment sites (att) and are required for integration into the host genome. The LTRs also serve as enhancer-promoter sequences, controlling expression of the viral genes. The LTRs (U3-R-U5) consist of untranslated regions (U), which contain the transcription start site, a polyadenylation signal, and repeated sequences (R) important for reverse transcription. Other critical elements in the viral genome include the packaging sequence (psi, ψ), which interacts with capsid proteins during packaging and allows the viral RNA to be distinguished from other RNAs in the host cells, and the primer binding site (PBS) and polypurine tract (PPT) adjacent to the 5' and 3' LTR, respectively, both of which are essential for reverse transcription. Once integrated, the proviral genome will synthesize a full-length viral transcript using host RNA polymerase. The full-length viral transcript encodes the viral Gag-Pol polyprotein that provides the capsid and enzymes for reverse transcription (reverse transcriptase) and integration (integrase). The synthesis and nuclear export of the full-length viral RNA require the interaction of viral regulatory proteins with different cis-acting sequences in the viral RNA. All lentiviral regulatory and accessory proteins are encoded by variously spliced viral mRNAs that are generated from this full-length viral RNA using different 5' and 3' splice site signals (Fig. 1). The two essential regulatory proteins, Tat


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Fig. 2. Plasmid constructs for the generation of HIV-1-derived lentiviral vectors. The HP/TV lentiviral vector system uses three basic vector constructs, pHP, pHEFVSVG, and pTY in DNA cotransfections. An additional eukaryotic expression plasmid, pCEP4-tat, can be included that increases vector titer two to fivefold (14). pHP expresses all viral proteins except for Env and Nef. pTY is a self-inactivating (SIN) transducing vector derived from pTV carrying necessary lentiviral packaging signals (ψ). Insert: Electron microscopic photograph of concentrated HP/TV vectors mixed with 142 nm latex beads (white particles).

and Rev, are required for efficient Gag-Pol synthesis. Tat interacts with a 59-nt RNA structure, TAR, at the 5' end of the viral RNA and promotes transcriptional elongation. Rev facilitates nuclear export of unspliced and singly spliced viral RNA by interacting with Rev responsive element (RRE) and other cisregulatory sequences (1). Although the accessory genes of HIV-1 have been shown to be dispensable for lentiviral vector function (8,9), their possible roles in transduction of different types of cells have not been extensively studied. For example, there is evidence that the vpr gene is needed for efficient transduction of resting Tcells (10).

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1.2. A Simple Lentiviral Vector System: Three Plasmids Plus a Human Cell Line The vector system described here is based on HIV-1 (see Chapters 19 and 20). However, lentiviral vector systems based on simian immunodeficiency virus (SIV), FIV, and EIAV have also been established (11–13, and Chapters 23 and 24). The production of HIV-1-derived lentiviral vectors requires human cell lines because many of the viral regulatory functions are human cell dependent. Lentiviral vectors can be produced by cotransfection of the three different plasmid constructs coding for Gag-Pol, VSV-G envelope, and the vector genome (Fig. 2). An ideal vector system will have these components established separately without overlapping sequences. The helper construct of the lentiviral vector system, pHP, contains a chimeric promoter that drives expression of Gag-Pol. pHP has deletions in the 5' untranslated leader, env, nef, and the 3' LTR (14). Besides Gag-Pol, pHP also produces Tat, Rev, and other HIV1 accessory proteins (Vif, Vpr, and Vpu) through RNA splicing. The complicated gene regulation scheme of lentivirus makes it difficult to express gag-pol independent of Tat, Rev, and cis-regulatory elements. Although Tat- and Revdependent lentiviral vectors have been generated, extensive testing of these vectors has not been reported. Several cis-acting sequences are required for gag-pol expression and are located across the entire viral genome (15–18). The deletion of these sequences from the helper vector construct diminishes gagpol expression. In addition, constitutive expression of HIV-1 Gag-Pol and other viral proteins has been shown to be toxic to cells (see ref. 19 and Chang, unpublished data). The problems associated with the synthesis of lentiviral Gag-Pol have slowed the development of a stable high-titer vector system. The transducing construct, pTV, which serves as a vehicle for foreign gene delivery, was derived from an LTR-modified recombinant HIV-1 plasmid (20). Lentiviral LTRs are transcriptionally silent without Tat. This means that the 5' LTR of pTV cannot be used as a functional promoter to drive foreign gene expression as commonly applied with the 5' LTR of MLV vectors. Nevertheless, to improve safety, efficacy, and viral titer, a self-inactivating (SIN) lentiviral vector (pTY) has been generated with extensive deletions in 3' U3 and U5, as well as insertion of a strong polyadenylation signal (21). In pTY, the gene of interest under control of its own enhancer/promoter should be inserted downstream of RRE, which is needed for efficient genomic RNA expression and packaging. The transducing constructs of lentiviruses require more than the conserved retroviral packaging signal (ψ) for efficient packaging. Sequences in TAR, gag, RRE, and env have all been reported to effect HIV-1 genome packaging (22–25). In addition to pHP and pTY, a VSV-G expression construct, pHEF-VSVG, is needed for the synthesis of the viral envelope. The construct pHEF-VSVG


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uses a strong human elongation factor promoter to drive expression of VSV-G. Control of VSV-G levels may be necessary to reduce vector toxicity. 1.3. Safety Issues Concerning Lentiviral Vectors Because lentiviruses are potentially lethal human pathogens, efforts must be made in the development of lentiviral vector systems to minimize the risk of replication-competent virus (RCV) production. This is best achieved by deleting or replacing viral sequences from the vector constructs. Sequences such as env, accessory genes, and most of the 3' U3 and U5 can be deleted without affecting vector function. Additional safety steps should be taken by constantly monitoring RCV production. Since lentiviral transducing vectors do not carry any viral genes, the expression of gag-pol would signal RCV production. The most sensitive assay for RCV detection is the polymerase chain reaction (PCR). PCR is very sensitive, but the results are easily confounded by the presence of plasmid DNA. Another simple and sensitive method for detecting RCV is to use immunostaining to detect Gag expression. For example, HIV-1 Gag p24 expression can be detected at the single-cell level using anti-p24 antibodies (14). Production of RCV of HIV-1-derived vectors can also be monitored by coculturing with cell lines that are sensitive to infection and spread of the virus. Alternatively, culture supernatant can be assayed for HIV-1 reverse transcriptase (RT) activity (20). An active program of RCV monitoring should be established by all viral vector production facilities. 1.4. Applications of Lentiviral Vectors: Problems and Possible Solutions 1.4.1. Insertion and Expression of Foreign Genes A foreign promoter/gene cassette of up to 8–9 kb can be inserted into the transducing vector pTY. Our recent studies suggest that the pTY transducing vector does not contain silencing or destabilizing elements, which are found in conventional retroviral vectors that affect long-term gene expression (see refs. 26 and 27 and Zaiss and Chang, unpublished data). The expression of lentiviral transgenes has been shown to be sustained in vitro and in vivo for over 6 months (14,28). 1.4.2. Titer, Stability, and Toxicity of Lentiviral Vectors The key to production of large quantities of lentiviral vectors is to increase the per cell production level of the vectors. With optimal transfection conditions, up to 107 infectious units per mL, or approx 100 infectious units per cell can be produced in 24 h. For high-titer and scale-up production of lentiviral

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vectors, a high-titer producer cell line needs to be developed that will also reduce the risk of RCV production. A few lentiviral producer cell lines based on the tetracycline inducible system have been reported, but their stability and consistency of long-term, high-titer production await further evaluation (29–31 and see Chapter 20). VSV-G pseudotyped vectors are sensitive to human serum, which may present some problems in future systemic in vivo lentiviral vector delivery (32,33). In addition to serum sensitivity, in vivo distribution of vector particles is also a rate-limiting step. These physical barriers may be overcome by modifications of lentiviral transduction protocols. The toxicity of lentiviral Gag-Pol (HP), VSV-G (env), or other viral proteins may affect both vector production and its use (see Subheading 1.4.3.). This problem might be confounded by the high defective particle ratios with the HIV-1-derived vectors, which are approx 346:1 (particle: infectious unit) with unconcentrated vector stocks and approx 18:1 with the concentrated vector stocks (33). Improvement of the defective particle to infectious unit ratio may increase the efficiency of vector transduction and reduce toxicity. 1.4.3. In Vitro and In Vivo Use of Lentiviral Vectors In vivo lentiviral transduction of brain, eye, liver, and muscle tissues of mice or rats has been demonstrated (34–37). Although VSV-G pseudotyped lentiviral vectors have expanded host cell tropism, efficient transduction of different tissue targets remains cell type and growth state dependent. Cells of different vertebrate species (including chicken, mouse, rat, monkey, and human) and of different tissue origins and growth states (including neural cells, pancreatic islets, retina, muscles, macrophages, dendritic cells, fibroblasts, endothelial cells, activated T-cells, embryonic stem cells, and different tumor cell lines) have been successfully transduced with lentiviral vectors (11,14,36,38,39). However, efficient transduction of CD34 hematopoietic stem cells, nonproliferating hepatocytes, monocytes, resting T-cells, some primary tumor cultures, and mouse T-cells with the VSV-G pseudotyped lentiviral vectors has been limited or requires high multiplicity of infection (MOI) (see refs. 11,40–43 and Chang, unpublished data). Pseudotyping with chimeric or alternative viral envelopes may overcome the entry barriers. Efficiency of transduction may also be improved by treating the target cells with growth factors. For example, transduction of primary resting T-cells has been successfully demonstrated by supplementing with cytokine interleukin (IL)-2, IL-4, IL-7, or IL-15 in the culture (41,44).


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2. Materials 2.1. Cells and Culture Conditions 1. 293, 293T-cells (transformed human primary embryonic kidney cells) and TE671 cells (human rhabdomyosarcoma cells) can be obtained from American Type Culture Collection (ATCC), Rockville, MD. 2. Cells are maintained in Dulbecco’s modified Eagle’s medium (DMEM; Mediatech) supplemented with 10% fetal bovine serum (FBS; Gibco BRL) and 100 U/mL of penicillin-streptomycin (Gibco BRL). 3. Stock cells are maintained in T75 flasks and split 1/6 every 3–4 days. These cells should not be overgrown at any time. 4. 6-well tissue culture plates for transfection and 24-well plates for titration.

2.2. Plasmids 1. All plasmids used for transfection are purified by CsCl gradient centrifugation (see Note 1). 2. The two expression plasmids, pHP and pHEF-VSVG, which encode HIV-1 structural protein Gag-Pol and VSV-G envelope, respectively, provide necessary helper functions. The third plasmid, pTV or pTY (SIN vector), carries the transgene of interest (promoter plus the transgene open reading frame). A polylinker cloning vector, pTVlinker, or pTYlinker is available for easy insertion of foreign genes (see Note 2). 3. To increase vector titer (up to fivefold), a fourth plasmid, pCEP4Tat, which provides additional transactivation function, can be included in the DNA cotransfection.

2.3. DNA Transfection It is important that all materials be sterile to prevent tissue culture contamination. 1. 6-well-tissue culture plates, T25 flasks, or other culture dishes. 2. 15-mL polystyrene or polycarbonate but not polypropylene tubes. Polypropylene reduces the efficiency of DNA transfection. 3. Sterile ddH2O (see Note 3). 4. 2.5 M CaCl2 (Mallinkrodt brand; see Note 4). 5. 2× BBS (BES-buffered solution): 50 mM N,N-bis(2-hydroxyethyl)-2 aminoethanesulfonic acid (BES; Calbiochem or Sigma), 280 mM NaCl, 1.5 mM Na2HPO4; adjust the pH with 1 N NaOH to precisely 6.95. Filter the 2× BBS solution with a 0.45-μm filter and freeze in aliquots at –20°C (see Note 5).

2.4. Viral Vector Harvesting and Concentration 1. Sarstedt 1.5-mL sterile screw-cap tubes and 15- and 50-mL conical tubes. 2. 0.45-μm, sterile-packed, low-protein-binding filters (Millex-HV, Millipore). 3. Polyethylene glycol 8000 (PEG 8000), 50% stock in ddH2O, autoclaved.

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4. NaCl, 5 M stock, autoclaved. 5. Microfuge (max. 20,000g) and bench top clinical centrifuge (max. 4100g).

2.5. Lentiviral Vector Titration for LacZ Reporter Gene Expression 1. 2. 3. 4.

24-well tissue culture plates. Polybrene (Sigma), 10 mg/mL stock (1000×), filter sterilized. Phosphate-buffered saline (PBS). Fixation solution: 1% formaldehyde (0.27 μL of 37.6% stock to make 10 mL), 0.2% glutaraldehyde (Sigma, 80 μL of 25% stock to make 10 mL) in PBS. 5. X-gal-staining solution: 10 mL solution of PBS containing 4 mM K-ferrocyanide (100 μL of 0.4 M stock), 4 mM K-ferricyanide (100 μL of 0.4 M stock), 2 mM MgCl2 (20 μL of 1 M), and 0.4 mg/mL X-gal (200 μL of 20 mg/mL stock in dimethyl formamide). Stock ferrocyanide, ferricyanide, and X-gal should be kept frozen and away from light (see Note 6).

3. Methods 3.1. Generation of Recombinant Lentiviral Vectors Viral vectors are generated by cotransfection of three or four plasmids into 293, 293T or TE671 cells (Fig. 3). TE671 cells are easier to handle because they attach to the culture dish better than 293 cells. All the following steps should be carried out in a biosafety hood. Lentiviral vectors should be handled using NIH BSL-2 safety guidelines. Extra caution should be taken if one is not familiar with the vector background and the monitoring procedures for RCV. 3.1.1. Cell Preparation 1. 17–20 h before transfection, seed each well of a 6-well plate with 7 × 105 TE671 cells in 2 mL DMEM. By the time of transfection, the culture should have reached 95–100% confluency. (Cells can also be split in T25 flasks with 5 mL complete DMEM; see Note 7). 2. The cells should be fed with fresh medium prior to adding the DNA. This can be done during DNA incubation time.

3.1.2. DNA Transfection Using Calcium Phosphate Precipitation Method 1. Wipe-clean a test tube rack and pipetmans with 70% ethanol. Prepare one polycarbonate tube per vector sample. 2. For each well of a 6-well plate, pipette sterile ddH2O 90 μL and 2.5 M CaCl2 10 μL into one tube, and mix by vortexing (see examples in Fig. 4). Add the following amount of DNA (2 μg/μL DNA stocks) to each tube:15 μg pHP, 3 μg pHEFVSV-G, 8 μg pTV (or pTY), and an optional 0.5 μg pCEP4Tat. Optional: a control


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Fig. 3. A simple flow chart depicting lentiviral vector production. The HP/TV vector system uses three DNA constructs for cotransfection of TE671 cells in 6-well plates.

3.

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5. 6.

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plasmid can be included in the DNA mixture for monitoring transfection efficiency, for example, a GFP expression plasmid if the pTV construct does not express GFP. To the DNA solution for each well, add 100 μL of 2× BBS buffer at 2–3 drops each time with gentle shaking while adding the buffer. A fine precipitate will form immediately after mixing DNA with the BBS buffer (see Note 8). Incubate at room temperature (RT) for 5–45 min depending on the turbidity (pale white suspension) of the DNA solution. If the DNA precipitates form quickly and the solution looks very turbid, allow the solution to sit at RT for only 5–10 min before adding it to the culture well. During DNA-calcium phosphate incubation, replace the culture medium with 2 mL fresh medium (see Note 9). Add the DNA precipitate (200 μL/well) dropwise while swirling the plate with the other hand. If DNA is added too fast, the strong local pH changes may result in reduced transfection efficiency. Incubate the culture plates overnight at 37°C in a 3% CO2 incubator, which further improves transfection efficiency.

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Fig. 4. Examples of producing two different lentiviral vectors. The diagram shows the production of two different lentiviral vectors, A and B, scaled for 3-well and 2well transfections, respectively, using a 6-well tissue culture plate.

3.2. Viral Vector Harvesting and Concentration 3.2.1. Harvesting Virus 1. The next morning (15–20 h after DNA addition), remove the medium, wash the cells once with 1–2 mL medium if necessary, and add fresh medium (1–2 mL). At least 70–80% cells (up to 100%) should express the cotransfected green fluorescence protein (GFP), which can be monitored directly under an inverted fluorescent microscope. 2. The virus is secreted into the medium. From this time point on (15–20 h after DNA addition), virus can be harvested every 12 h for 3–4 days by collecting the cell culture medium. The highest titer falls in between the second and the fifth harvest (see Note 10). 3. For unconcentrated virus stocks, virus supernatant is filtered using a 0.45- or 0.2-μm low-protein-binding filter to remove cell debris. Virus aliquots should be stored at –80°C until use (extended exposure to RT or repeated freezing and thawing reduces the titer). The transfected cells normally produce lentiviral vectors with titers ranging from 105 to 106 transducing units per milliliter of culture medium. 4. For concentrated virus preparation, virus supernatant can be pooled and frozen at –80°C immediately after collection for later concentration use.

3.2.2. Lentiviral Vector Concentration by Microfuge Centrifugation A small volume of lentiviral vectors can be concentrated 30–50-fold by a simple centrifugation protocol using a microcentrifuge. 1. Filtered virus supernatant is transferred as a 1-mL aliquot into a 1.5-mL sterile screw-cap tube with one side marked with a marker (Sarstedt) (see Note 11). 2. With the marked side facing out, spin the tube at 20,000g at 4°C in a microfuge for 2.5 h.


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3. Carefully transfer the tubes to a biosafety hood and discard most of the supernatant by pipeting, but leave behind approx 20–30 μL vol. 4. Rigorously vortex each tube for 20 s and then vortex gently and continuously at 4°C in a mixer or shaker for 2–4 h or overnight. 5. The same vector sample should be pooled and realiquoted to avoid titer variations among different tubes. The virus aliquots should be stored at –80°C.

3.2.3. Concentration by PEG 8000 Precipitation For a large volume of virus concentration, we recommend the PEG 8000 precipitation method. The protocol is quite gentle to lentivirus, and the recovery is close to 100%. The only drawback is the presence of a high concentration of PEG in the final virus pellet, which may affect subsequent operations. However, most tissue culture cells are not affected by the low volume of PEG in the concentrated virus stock. 1. Centrifuge the collected virus supernatant at 2500g for 10 min to remove dead cell debris, filter the supernatant through a 0.45- or 0.2-μm low-protein-binding filter into a 50-mL conical tube, and keep on ice. 2. To the virus supernatant, add 50% PEG 8000 to a final 5%, and leave on ice. 3. To the virus-PEG sample, add 5 M NaCl to a final 0.15 M, and mix by inverting the tube several times. 4. Incubate the virus and PEG mix on a rotating wheel at 4°C overnight. 5. After overnight incubation, centrifuge the virus-PEG mix in a bench top clinical centrifuge at 4100g for 10 min. 6. Discard the supernatant carefully so as not to disturb the white virus-PEG pellet. 7. The virus pellet can be resuspended in any desired buffer at low volume (usually at 1/100 of the original sample volume). The pellet can be easily dissolved in PBS or any buffer solution by gently pipeting up-and-down. 8. The virus stock can be stored at –80°C in small aliquots.

3.3. Titration of Lentiviral Vectors Carrying a lacZ Reporter Gene The titration assay described below and in Fig. 5 determines the number of infectious units per mL of virus carrying the lacZ reporter gene. 1. Split TE671 cells at 6 × 104 cells/well in a 24-well plate (approx 90% confluent). Allow cells to attach to the plate (2–4 h to overnight). 2. Mix different volumes of virus stock (usually 2–20 μL for virus with expected titer of 105–106/mL) with 200–300 μL growth media containing 4–8 μg/mL Polybrene. 3. Add the diluted virus to each well and incubate the plate at 37°C in a 5% CO2 incubator overnight. 4. The next morning, add 0.5 mL growth media to each well and incubate the plate for another 24 h. (Incubation time can be up to 48 h from the time the virus was added.)

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Fig. 5. Titration of lentiviral vectors carrying a lacZ reporter gene. The diagram illustrates titer determination by using different dilutions of a concentrated lacZ reporter vector stock on TE671 cells in a 24-well tissue culture plate. 5. For lacZ enzyme assay, wash cells twice with PBS, and fix at room temperature with the fixative for exactly 5 min (300 μL/well). 6. Wash cells 3 times with PBS, add 300 μL X-gal staining solution to each well, and incubate the plate at 37°C overnight (see Note 6). 7. Determine virus titer by counting blue cells directly using an inverted microscope.

4. Notes 1. CsCl banding is necessary (45), because the quality of plasmid DNA is critical to transfection efficiency; purified DNA should be dissolved at 2 μg/μL in molecular biology grade ddH2O (BRL). 2. pHP, pTYlinker, pTYEFnlacZ, pTYEFeGFP, pHEF-VSVG, and pCEP4tat are all available from the NIH AIDS Research and Reference Reagent Program (http:// www.aidsreagent.org/). pHP transformed bacteria should be grown at 30°C during plasmid amplification to prevent deletion. For the transducing vector con-


3. 4. 5.

6.

7. 8.

9. 10. 11.

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struct (pTY or pTV), an internal promoter is necessary, but a foreign polyadenylation signal should not be included. The quality of water is critical to transfection. Molecular grade ddH2O should be used for the preparation of all buffers, media, and DNA solutions. Many other brands of CaCl2 do not work. The working stock of 2× BBS can be kept in room temperature, but the pH may change with time. Therefore, the DNA incubation time will need to be adjusted accordingly by monitoring the cloudiness of the DNA precipitates. The pH of the X-gal solution for ß-galactosidase assay is critical if the cells have background enzyme activity, which can be prevented by adjusting the reaction pH using Tris-HCl buffer pH 8.0–8.5. A consistent high titer is usually obtained from 6-well plate transfections. The pH of BBS is critical to the transfection efficiency. If the DNA solution remains very clear or becomes very turbid immediately after adding 2× BBS, the transfection efficiency will be low. A slightly turbid mixture, which becomes more turbid with time, signals the success of DNA precipitation. To ensure optimal pH, use a fresh bottle of medium (less than 1 month old) made with high quality ddH2O as noted above (Note 3). For harvest at 12-h periods, feed cells with a low volume of medium (1 mL/well of 6-well plates) to enrich virus concentration. Mark one side of the tube and remove medium from the other side of the tube after centrifugation to avoid disturbing the virus pellet.

References 1. Tang, H., Kuhen, K. L., and Wong-Staal, F. (1999) Lentivirus replication and regulation. Annu. Rev. Genet. 33, 133–170. 2. Verma, I. M. and Somia, N. (1997) Gene therapy—promises, problems and prospects. Nature 389, 239–242. 3. Fouchier, R. A. and Malim, M. H. (1999) Nuclear import of human immunodeficiency virus type-1 preintegration complexes. Adv. Virus Res. 52, 275–299. 4. Emi, N., Friedmann, T., and Yee, J. K. (1991) Pseudotype formation of murine leukemia virus with the G protein of vesicular stomatitis virus. J. Virol. 65, 1202–1207. 5. Burns, J. C., Friedmann, T., Driever, W., Burrascano, M., and Yee J.-K. (1993) Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to a very high titer and efficient gene transfer into mammalian and nonmammalian cells. Proc. Natl. Acad. Sci. USA 90, 8033–8037. 6. Coffin, J. M., Hughes, S. H., and Varmus, H. E. (1997) Retroviruses. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. 7. Emerman, M. and Malim, M. H. (1998) HIV-1 regulatory/accessory genes: keys to unraveling viral and host cell biology. Science 280, 1880–1884. 8. Zufferey, R., Nagy, D., Mandel, R. J., Naldini, L., and Trono, D. (1997) Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nat. Biotechnol. 15, 871–875.

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9. Haas, D. L., Case, S. S., Crooks, G. M., and Kohn, D. B. (2000) Critical factors influencing stable transduction of human CD34(+) cells with HIV-1-derived lentiviral vectors. Mol. Ther. 2, 71–80. 10. Chinnasamy, D., Chinnasamy, N., Enriquez, M. J., et al. (2000) Lentiviral-mediated gene transfer into human lymphocytes: role of HIV-1 accessory proteins. Blood 96, 1309–1316. 11. Poeschla, E. M., Wong-Staal, F., and Looney, D. J. (1998) Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors. Nat. Med. 4, 354–357. 12. White, S. M., Renda, M., Nam, N. Y., et al. (1999) Lentivirus vectors using human and simian immunodeficiency virus elements. J. Virol. 73, 2832–2840. 13. Olsen, J. C. (1998) Gene transfer vectors derived from equine infectious anemia virus. Gene Ther. 5, 1481–1487. 14. Chang, L.-J., Urlacher, V., Iwakuma, T., Cui, Y., and Zucali, J. (1999) Efficacy and safety analyses of a recombinant human immunodeficiency virus type 1 derived vector system. Gene Ther. 6, 715–728. 15. Olsen, H. S., Cochrane, A. W., and Rosen, C. (1992) Interaction of cellular factors with intragenic cis-acting repressive sequences within the HIV genome. Virology 191, 709–715. 16. Amendt, B. A., Hesslein, D., Chang, L.-J., and Stoltzfus, C. M. (1994) Presence of negative and positive cis-acting RNA splicing elements within and flanking the first tat coding exon of human immunodeficiency virus type 1. Mol. Cell. Biol. 14, 3960–3970. 17. Huffman, K. M. and Arrigo, S. J. (1997) Identification of cis-acting repressor activity within human immunodeficiency virus type 1 protease sequences. Virology 234, 253–260. 18. Mikaelian, I., Krieg, M., Gait, M. J., and Karn, J. (1996) Interactions of INS (CRS) elements and the splicing machinery regulate the production of Rev-responsive mRNAs. J. Mol. Biol. 257, 246–264. 19. Levy, J. A. (1993) Pathogenesis of human immunodefeciency virus infection. Microb. Rev. 57, 183–289. 20. Chang, L.-J., McNulty, E., and Martin, M. (1993) Human immunodeficiency viruses containing heterologous enhancer/promoters are replication competent and exhibit different lymphocyte tropisms. J. Virol. 67, 743–752. 21. Iwakuma, T., Cui, Y., and Chang, L. J. (1999) Self-inactivating lentiviral vectors with U3 and U5 modifications. Virology 261, 120–132. 22. Berkowitz, R. D., Hammarskjold, M.-L., Helga-Maria, C., Rekosh, D., and Goff, S. P. (1995) 5' Regions of HIV-1 RNAs are not sufficient for encapsidation: implications for the HIV-1 packaging signal. Virology 212, 718–723. 23. McBride, M. S., Schwartz, M. D., and Panganiban, A. T. (1997) Efficient encapsidation of human immunodeficiency virus type 1 vectors and further characterization of cis elements required for encapsidation. J. Virol. 71, 4544–4554. 24. Cui, Y., Iwakuma, T., and Chang, L. J. (1999) Contributions of viral splice sites and cis-regulatory elements to lentivirus vector function. J. Virol. 73, 6171–6176.


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25. Clever, J. L., Taplitz, R. A., Lochrie, M. A., Polisky, B., and Parslow, T. G. (2000) A heterologous, high-affinity RNA ligand for human immunodeficiency virus Gag protein has RNA packaging activity. J. Virol. 74, 541–546. 26. Kempler, G., Freitag, B., Berwin, B., Nanassy, O., and Barklis, E. (1993) Characterization of the Moloney murine leukemia virus stem cell-specific repressor binding site. Virology 193, 690–699. 27. Challita, P. M., Skelton, D., El-Khoueiry, A., et al. (1995) Multiple modifications in cis elements of the long terminal repeat of retroviral vectors lead to increased expression and decreased DNA methylation in embryonic carcinoma cells. J. Virol. 69, 748–755. 28. Blomer, U., Naldini, L., Kafri, T., et al. (1997) Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector. J. Virol. 71, 6641–6649. 29. Freundlieb, S., Schirra-Muller, C., and Bujard, H. (1999) A tetracycline controlled activation/repression system with increased potential for gene transfer into mammalian cells. J. Gene Med. 1, 4–12. 30. Kafri, T., van Praag, H., Ouyang, L., Gage, F. H., and Verma, I. M. (1999) A packaging cell line for lentivirus vectors. J. Virol. 73, 576–584. 31. Klages, N., Zufferey, R., and Trono, D. (2000) A stable system for the high-titer production of multiply attenuated lentiviral vectors. Mol. Ther. 2, 170–176. 32. Takeuchi, Y., Porter, C. D., Strahan, K. M., et al. (1996) Sensitization of cells and retroviruses to human serum by (alpha 1-3) galactosyltransferase. Nature 379, 85–88. 33. Higashikawa, F., and Chang L.-J. (2000) Kinetic analyses of stability of retroviral and lentiviral vectors. Virology 280, 124–131. 34. Miyoshi, H., Takahashi, M., Gage, F. H., and Verma, I. M.. 1997. Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector. Proc. Natl. Acad. Sci. USA 94, 10319–10323. 35. Kafri, T., Blomer, U., Peterson, D. A., Gage, F. H., and Verma, I. M. (1997) Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nat. Genet. 17, 314–317. 36. Blomer, U., Naldini, L., Kafri, T., et al. (1997) Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector. J. Virol. 71, 6641–6649. 37. Naldini, L., Blomer, U., Gage, F. H., Trono, D., and Verma, I. M. (1996) Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector. Proc. Natl. Acad. Sci. USA 93, 11382– 11388. 38. Miyoshi, H., Takahashi, M., Gage, F. H., and Verma, I. M. (1997) Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector. Proc. Natl. Acad. Sci. USA 94, 10319–10323. 39. Kafri, T., Blomer, U., Peterson, D. A., Gage, F. H., and Verma, I. M. (1997) Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nat. Genet. 17, 314–317. 40. Zack, J. A., Arrigo, S. J., Weitsman, S. R., et al. (1990) HIV-1 entry into quiescent primary lymphocytes: molecular analysis reveals a labile, latent viral structure. Cell 61, 213–222.

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41. Unutmaz, D., KewalRamani, V. N., Marmon, S., and Littman, D. R. (1999) Cytokine signals are sufficient for HIV-1 infection of resting human T lymphocytes. J. Exp. Med. 189, 1735–1746. 42. Park, F., Ohashi, K., Chiu, W., Naldini, L., and Kay, M. A. (2000) Efficient lentiviral transduction of liver requires cell cycling in vivo. Nat. Genet. 24, 49–52. 43. Case, S. S., Price, M. A., Jordan, C. T., et al. (1999) Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors. Proc. Natl. Acad. Sci. USA 96, 2988–2993. 44. Emerman, M. (2000) Learning from lentiviruses. Nat. Genet. 24, 8–9. 45. Maniatis, T., Fritsch, E. F., and Sambrook, J. (1989) Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.

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22 Simian Foamy Virus Vectors Preparation and Use Jeonghae Park and Ayalew Mergia

1. Introduction The life cycle of retroviruses involves stable integration of viral genetic material into the host genome; expression of viral genes is, in part, regulated by host cell factors (1). These features make retroviruses a widely used efficient means for introducing foreign DNA into the cell genome. Most retroviral vector systems used in clinical gene transfer are based on murine leukemia virus (MuLV) (2,3). MuLV replication is cell cycle dependent, and these vectors are inadequate to transduce nondividing and/or terminally differentiated cells stably, which severely restricts their potential utility for clinical gene transfer (4–6). In contrast, vectors based on the human immunodeficiency virus (HIV) can deliver genes into nondividing cells as efficiently as into proliferating cells (7,8). HIV vectors, then, serve as vehicles to deliver a gene of interest into clinically important terminally differentiated, quiescent, and nondividing cells. The use of vectors derived from a pathogenic virus for human gene therapy, however, remains a major safety concern and health risk issue. Recently, it was shown that animal lentivirus vectors pseudotyped with vesicular stomatitis virus envelope glycoprotein G (VSV-G) can transduce human cells, overcoming the restricted host tropism (9). These vectors deliver genes into nondividing cells as efficiently as HIV. However, the comparative safety and efficacy of vectors based on nonprimate lentiviruses in humans remain to be determined. Foamy viruses have several inherent features that make them an ideal alternative vector system for human gene therapy. These viruses are distinct and From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Differential gene expression by SFV-1. Top: schematic representation of the genetic organization of SFV-1 provirus. +1 at the arrow represents transcription initiation sites by the internal promoter located at the 3' end of env and U3 promoter of the 5' LTR. The arrow indicates direction of transcription. Early transcripts are controlled by the internal promoter located at the end of env and late transcripts by the U3 promoter. Tas is required for expression of the late transcripts. It is not clear whether there is a protein product is encoded by the orf-2 region.

grouped into the Spumavirus genus of retroviruses. Foamy viruses are ubiquitous and are found in many mammalian species. The virus can be propagated efficiently in various cell types of several species (10). Cultured epithelial and fibroblast cells as well as lymphoid and neurally originating cells support the growth of foamy viruses. Each foamy virus isolate can infect several mammalian species, and virus has been recovered from many organs in these animals (11). To date, no disease has been attributed to foamy virus in naturally or experimentally infected animals (12–15). Humans are not natural hosts of foamy virus infection and animal caretakers accidentally infected with simian foamy virus (SFV) remain healthy after more than 10 years of infection (16,17). Importantly, foamy virus vectors can deliver genes efficiently into nondividing cells and human peripheral blood lymphocytes (18). This chapter describes


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progress in vector development and practical aspects of foamy virus vector, focusing on the SFV-1 system. 1.1. Genomic Structure of Foamy Virus Foamy viruses possess a complex genomic organization as well as a complex means of regulating gene expression. The genome of SFV-1 is 11,671 nucleotides long and contains the structural genes gag, pro, pol, and env, which encode core proteins, protease, reverse transcriptase, integrase, and envelope protein, respectively (Fig. 1) (14,19). The long terminal repeat (LTR) of SFV1 is 1621 nucleotides in length, which is unusually long for retroviruses. In addition to gag, prt, pol, and env, SFV-1 contains two open reading frames (ORFs) located at the 3' end of env. In contrast, the genome of the human foamy virus (HFV) contains three ORFs in the corresponding region (20,21). Other primate foamy viruses, as well as bovine, feline, and equine isolates, have two ORFs similar to SFV-1 (22–26). The first ORF encodes a transcriptional transactivator designated tas (transcriptional transactivator of spumavirus) that activates gene expression directed by the viral promoters (22,27–32). It remains controversial whether there is a protein product encoded by the ORF-2 region (33–37). A Bet protein, which is a product of a spliced message containing the first 88 amino acids of the Tas fused to the last 390 amino acids of ORF-2, was found to be highly expressed in cytoplasm of foamy virus-infected cells (36,38–40). The function of bet has not been fully elucidated (37,41–43). 1.2. Overview of Foamy Virus Life Cycle Foamy viruses share many features with other retroviruses. These viruses also have distinct characteristics that make them unique among retroviruses. Viral gene expression is temporally regulated and controlled by different promoters like DNA viruses (Fig. 1). Similar to other retroviruses, the U3 domain of the LTR contains a promoter element. In addition, foamy viruses contain a second promoter located at the 3' end of env upstream from the tas gene (39,44– 46). Immediately after virus infection, the RNA genome is reverse transcribed into double-stranded DNA, which is then transported to the nucleus and integrates into the host genome. Viral gene expression commences with the internal promoter directing the expression of genes located at the end of env including tas. Following initial expression, Tas feedback on the internal promoter further amplifies the expression of regulatory genes (39,45). Subsequently, Tas acts on the LTR to express the virion structural genes (gag, prt, pol, and env). Newly synthesized viral genome and proteins assemble, and virus particles are formed by budding from the plasma membrane or mature inside the cell

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within vacuoles. Gag precursor protein is produced from unspliced genomic transcripts and Env from a singly spliced subgenomic message. Similar to retroviruses with a complex genomic organization, multiple splicing events are required to generate messages that encode the tas-ORF-2 regions of foamy viruses (38). One feature common to all retroviruses that is not shared by the foamy viruses is that the Pol protein is not synthesized as a Gag-Pro-Pol precursor polyprotein. Instead, the Pro-Pol gene product of foamy viruses is translated from a spliced subgenomic message that lacks the Gag domain (47,48). Translation of the protease-polymerase products is initiated from an ATG initiator codon located at the 5' end of the protease gene (49,50). Distinct from other retroviruses, a second reverse transcription can occur late in the foamy virus replication cycle prior to virion release (58,51,52). About 20% of foamy virus particles were shown to contain double-stranded DNA, suggesting that foamy viruses have a distinct replication pathway with features of both retroviruses and hepadnaviruses. DNA isolated from the virion was shown to be infectious implying that fully reverse-transcribed DNA can be incorporated into virus particles (52). Mutational analysis in foamy viruses revealed that the tas gene is essential for viral replication, whereas ORF-2 is dispensable (33,34,53). Therefore, in addition to the four basic genes (gag, prt, pol, and env) and cis-acting elements required for virus replication, the tas gene is critical for foamy virus vector construction, but the ORF-2 region is dispensable. 1.3. Development of Foamy Virus Vector The first foamy virus vector was constructed by replacing a portion of the ORF-2 region with a foreign gene (54). This vector is replication competent and is capable of transducing genes efficiently. Replication-defective foamy virus vectors have also been constructed by replacing the env gene and/or tas ORF-2 region with a marker gene (53,55–60). For these vectors, the env and tas gene products were supplied in trans to express the vector genome and produce packaged vector particles that can infect target cells. Titers ranging from 103 to 105 can easily be obtained with these foamy virus vectors. Traditional retroviral vectors with a minimal genome sequence contain the 3' and the 5' LTRs, the cis packaging sequences, and the polypurine tract, which is required for the second DNA strand synthesis during reverse transcription of the RNA genome (2). Sequences important for packaging are usually located in the 5' leader region extending into the 5' end of the gag gene. The polypurine tract is mainly located upstream from the 3' LTR. A cis-acting element at the 3' end of the pol gene is critical for foamy vector-mediated gene transfer (58–60). The requirement of a second cis-acting element located in the pol gene for foamy virus vector is unique among retroviruses. Therefore, foamy virus vector construction with minimal genome requires the 3' and the 5' LTRs, the 5'


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leader region extending to the 5' gag, the cis-acting element in the pol gene, and the polypurine tract. Since the LTR depends on Tas for gene expression, the tas gene can be included in the vector or supplied in trans. Replacing the 5' U3 region of the LTR with the powerful cytomegalovirus (CMV) immediate early gene promoter can eliminate the need for Tas in foamy virus vector construction (61–64). In fact, in a number of retroviral vectors production of high-titer helper-free particles can be obtained utilizing the CMV promoter to drive the expression of both the packaging components and the vector genome (65–67). This system takes advantage of high-level transfectability and strong E1A-mediated stimulation of CMV-programmed transcription of the human embryonic kidney fibroblast-derived 293 cell line. The SFV-1 vector system, in which both the vector genome (pCV7-9) and the packaging plasmid (pCGPET) are placed under the control of CMV promoter, yields vector particles with titers up to 5 × 106/mL (63). One potential problem with retroviral vectors is generating replication-competent genome as a result of recombination between the vector and the packaging system. A foamy virus vector system that lacks the tas gene is restricted to one round of replication even if recombination occurs between the vector and packaging constructs. This feature makes foamy virus an ideal safe vector system for gene therapy. 1.4. SFV-1 Vector System Several versions of the SFV-1 vector containing the lacZ gene are available that effectively transduce a variety of cells from different species (58,63). Vector pCV7-9 (Fig. 2) is commonly used to test the efficiency of the SFV-1 vector system. In pCV7-9, the vector genome is constitutively expressed from the CMV promoter. This vector contains SFV-1 sequences from the beginning of the R to the end of the pol gene, the PPT, and the 3' LTR. To monitor for the efficiency of transduction, a lacZ gene under the control of CMV promoter is placed between the pol gene and PPT. Packaging plasmid (pCGPET) for SFV1 vector is constructed by placing the structural genes gag, pol, env, and tas downstream from the CMV promoter (63). A splice donor of the 5' SFV-1 is provided between the CMV promoter and the gag gene in pCGPET. The SV40 polyA signal sequence is supplied at the 3' end. Recombination between pCGPET and pCV7-9 could result in the production of wild-type virus. To restrict replication to one cycle in case of recombination, a mutation is introduced in the pCGPET, creating a Tas-defective packaging plasmid (pCGPEΔT) (Fig. 2). A further modified SFV-1 packaging system is available in which the gag-pol and env viral coding regions are on separate expression plasmids (63). Although this packaging system significantly reduces the chances of generating wild-type virus, there may be a decrease in vector production. Since Tas is critical for SFV-1 replication, the pCGPEΔT packaging system solves the prob-

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Fig. 2. SFV-1 vector and packaging constructs: SFV-1 provirus (A) and vector (B) and packaging (C) derivatives. CMV-lacZ is the coding sequence of the lacZ gene linked to the CMV immediate-early gene promoter. SD represents a synthetic DNA containing the 5' end of the SFV-1 splice donor cloned downstream from the CMV promoter.

lems of potential reduction in vector production caused by placing the structural genes in a separate plasmid and generating recombinant wild-type virus that spreads efficiently. 1.5. Packaging Cell Lines Foamy viruses cause extensive cytopathology in cell culture. The cytopathic effect includes cell fusion, potentially mediated by the interaction of the env gene product and cell receptor. Establishing a packaging cell line for foamy virus vector in which sufficient amounts of viral proteins are synthesized for efficient vector production without toxicity to the cells can be a major obstacle in foamy virus vector development. Recently, two packaging cell lines were created for SFV-1 vector using the human kidney embryonic fibroblast-derived 293 cell line: helper DNA is placed under the control of either a constitutive CMV immediate early gene or inducible tetracycline (tetO) promoter for expression (63). Transfection of pCV7-9 vector in the constitutive expressing and inducible cell lines produced SFV-1 vector particles with titers of 3.5 × 103 and 1.1 × 104 per mL, respectively. This level of vector production is several fold lower compared with transient vector expression when packaging and vector plasmids are cotransfected into 293T cells. Therefore, the 293T cell line will be an alternative for creating a packaging cell line that yields high-titer


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vector particles. The availability of stable packaging cell lines would allow a scale-up of production of vector stocks for gene therapy. 2. Materials 2.1. Cell Culture 1. Human embryonic kidney fibroblast-derived 293T cells. Cells are passaged by splitting 1:10 every 3–4 days. 293T cells can be obtained from American Type Culture Collection (Rockville, MD). 2. Fetal bovine serum (FBS). 3. Dubelco’s modified Eagle’s medium (DMEM). 4. Complete DMEM medium: DMEM with 10% FBS, 2 mM L-glutamine, 100 μg/mL, penicillin G and 100 μg/mL streptomycin. 5. Tissue culture flasks: 25 and 75cm2. 6. Hanks’ balanced salt solution (HBSS). 7. Trypsin-EDTA: 0.05% trypsin, 0.53 mM EDTA in HBSS. 8. A 37°C cell culture incubator under 5% CO2 conditions.

2.2. Recombinant SFV-1 Plasmid Vector To produce a pure plasmid of pCV7-9 vector for transfection, the DNA should prepared by CsCl gradient centrifugation. Alternatively, pure plasmid DNA can be prepared using a commercial Qiagen (Chatsworth, CA) plasmid preparation kit. It is always advisable to check purified plasmid by several restriction enzyme digestions to test for a possible deletion and/or rearrangements. A modified pCV7-9 vector is available with a unique SmaI site for cloning a foreign gene cassette upstream of the CMV-lacZ region. 2.3. Packaging Plasmid Construction of the packaging plasmid pCGPEΔT is described in Subheading 1.3.1. Packaging plasmid DNA should also be prepared by CsCl gradient purification or a Qiagen plasmid preparation kit. 2.4. Generation of Recombinant Virus 1. 2. 3. 4. 5. 6. 7. 8.

6-well cell culture plates. Lipofectamine and Opti-MEM medium (Gibco-BRL). Sodium butyrate (Sigma). Recombinant SFV-1 vector and packaging plasmid (see Subheadings 2.2. and 2.3.). DMEM and complete DMEM medium (see Subheading 2.1.). Phosphate-buffered saline (PBS): 1.0% NaCl, 0.025% KCl, 0.14% Na2HPO4, 0.025% KH2PO4. Filters (0.45 μm; Millipore). Disposable syringes (3 mL).

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2.5. Titration of Recombinant Virus 1. 2. 3. 4.

12-well tissue culture dishes. Complete medium (see Subheading 2.1.). PBS. X-gal solution (1 mg/mL 5-bromo-4-chloro-3-indoyl-β-D-galactopyranoside in 2 mM MgCl2, 5mM K4Fe[CN]6.3H2O, and 5 mM K3Fe(CN)6 in 1× PBS). 5. 0.25% glutaraldehyde (Sigma).

2.6. Infection of Nonadherent Cells with SFV-1 Vector Particles 1. 2. 3. 4. 5.

12-well culture plates. Microscope slides. Cytofunnel (Shandon, Pittsburgh, PA). Cytospin cytocentrifuge (Shandon, Pittsburgh, PA). RPMI-1640 medium with 10% FBS.

3. Methods 3.1. Generation of Recombinant Virus Recombinant virus can be produced by cotransfection of viral vector and packaging plasmid. We found that transfection in 293T cells yields the highest vector production. Vector particles can also be generated by transfection of the packaging cell line 293-2 or 293-24 (63) with viral vector plasmid. However, the vector production is significantly lower compared with that of particles harvested from 293T cells cotransfected with vector and packaging plasmids. The packaging cell lines 293-3 and 293-24 are derived from the 293 cell line. It is our experience that during transfection the 293T cells adhere better to the plate, whereas the 293 cells tend to lift from the surface of the culture dish; as a result, 293T cells yield several fold higher vector production. Therefore, we routinely prepare SFV-1 vector by cotransfecting pCV7-9 and pCPGEΔT into the 293T cell line 3.1.1. Transfection of DNA Using Lipofectamine The transfection procedure provided here is slightly modified from the Lipofectamine-mediated transfection method suggested by the manufacturer (see Note 1). To enhance expression of both vector genome and viral structural proteins, cells can be treated with sodium butyrate after transfection (see Note 2). 1. In a 6-well plate, seed 4 × 105 cells (293T cells) per well in 2 mL of DMEM with 10% FBS (see Note 3). 2. Incubate the cells at 37°C under 5% CO2 conditions until the cells are 80% confluent. This usually takes 24–48 h.


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3. For each transfection, dilute 9 μL of Lipofectamine reagent in 50 μL of OptiMEM. 4. Simultaneusly, for each transfection, dilute 1–3 μg (1.5 μg each of vector pCV79 and packaging pCGPEΔT) of DNA into 50 μL Opti-MEM and incubate for 30 min at room temperature. Peak activity should be at about 9–15 μL of Lipofectamine reagent for 3 μg DNA. 5. Allow diluted Lipofectamine and DNA to stand at room temperature for 30 min. 6. Mix the two solutions, vortex for 2 s at medium speed, and incubate for 30-45 min at room temperature to allow DNA-lipid complex formation. The solution may appear cloudy; however, this will not impede the transfection. 7. Wash the cells once with 2 mL of serum-free DMEM. 8. For each transfection, add 0.8 mL of serum-free DMEM to each tube containing the DNA-lipid complexes. Do not add antibacterial agents to media during transfection. Then slowly add the mix dropwise to each well of the plate containing the 293T cells. 9. Incubate the cells overnight (but not for a full 24 h) at 37°C in a 5% CO2 incubator. 10. Replace media the next morning with 1–1.5 mL DMEM containing 10 mM sodium butyrate. Cells must be 80–90% confluent before adding sodium butyrate. Maintain in sodium butyrate for 8–12 h (see Note 4). 11. Wash cells with HBSS and replace media after 8–12 h with complete DMEM medium. 12. Maintain cells for 4–5 days prior to harvesting supernatant. Filter harvested vector particles through 0.45-μm filters and store at –80°C. 13. Transfection efficiency can be checked by staining the cells for β-galactosidase (β-Gal) expression as described in Subheading 3.1.2. after harvesting the supernatant. We find that >70% cell transfection results in vector productions with titers ranging 5 × 105 to 5 × 106/mL vector particles (see Note 5).

3.1.2. Titration of SFV-1 Vector by β-Galactosidase Activity Assay Since the pCV7-9 vector carries the lacZ gene as a marker SFV-1 vector, stocks can be titered by infecting 293T cells and assaying for β-Gal activity. 1. In a 12-well tissue culture plate seed 2 × 105 293T cells and incubate cells at 37°C until the culture reach 80% confluence (24–48 h). 2. On the day of infection, prepare a 10-fold serial dilution of the vector stock using complete DMEM medium in a total volume of 300 μL for each dilution. 3. The cell culture at this point should be at least 80% confluent. Remove medium from the day-old cell culture and add each of the 300 μL vector diluents to each well. Incubate the cultures overnight at 37°C under 5% CO2 conditions. 4. Replace the medium with fresh complete DMEM and incubate for 2 more days in a 37°C cell culture incubator. 5. Wash cells twice with 0.5 mL of 1× PBS. 6. Fix the cells by adding 0.5 ml/well of 0.05% gluteraldehyde. Incubate at room temperature for no longer than 15 min.

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7. Remove the gluteraldehyde solution and gently rinse the cells three times with 1× PBS. 8. Add 0.5 mL fitered X-gal solution (1 mg/mL X-gal, 2 mM MgCl 2, 5mM K4Fe[CN]6.3H2O, and 5 mM K3Fe[CN]6 in 1× PBS). 9. Incubate cells at 37°C for 2–15 h to visualize the blue-stained cells, and count positive cells under a light microscope.

3.2. Infection of Nonadherent Cells For nonadherent cells such as primary and established lymphoid cells, we found higher transduction efficiency when infection is carried out by a spin inoculation method. The infection procedure provided for nonadherent cells is a modification of the method described previously (68,69). 1. Seed established nonadherent cells at a density of 3.5 × 104 in 24-well culture plates. Primary cells such as peripheral blood lymphocytes are plated at a density of 5 × 105 are plated for infection. 2. The following day centrifuge the cells briefly at 1500g for 10 min. 3. Remove medium carefully and resuspend cells in 200–300 μL vector supernatant. Multiplicity of infection (MOI) should be at least 1 for efficient gene transduction. 4. Spin the resuspended cells for 1–2 h at 1000g at room temperature and maintain in a 37°C cell culture incubator. 5. After 8 h repeat steps 2–4 and incubate at 38°C overnight. 6. Spin cells at 1500g for 10 min the next day, remove supernatant carefully, and add fresh medium. Incubate cells at 37°C for 48 h. 7. Transfer 200 μL of resuspended cells to a microscope slide by cytospin for 10 min at room temperature. 8. Make a circle around the cytospun cells with a water-repellent pen. 9. Rinse cells with PBS twice and fix with 200 μL of 0.05% gluteraldehyde for 15 min at room temperature. 10. Rinse cells with PBS 3 times, and add X-gal solution. Incubate slides at 37°C in a humidified chamber overnight. 11. Place cover slip after rinsing with PBS and score blue cells for transduction under a light microscope.

4. Notes 1. Among several transfection protocols we tested, including the CaPO4 procedure, the Lipofectamine method with the reagent from Gibco-BRL gives the least variability, and the transfection efficiency is reproducible. 2. Sodium butyrate has been shown to increase retroviral vector production by enhancing LTR or CMV promoter activity (70–72). 3. Each cell line has a unique seeding concentration that is important to transfection efficiency. A preliminary test determining the right seeding density for each cell line may be required for optimum transfection efficiency.


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4. Incubation time for sodium butyrate should not exceed 12 h. Cells transfected with the MuLV vector system survive 10 mM sodium butyrate concentration for 24 h. Incubation of SFV-1 vector-transfected cells in 10 mM sodium butyrate for 24 h, however, results in cell death. 5. Virus titer can be increased fivefold by combining cell-associated vector particles with that of supernatants. Foamy virus matures within the cell or by budding through the plasma membrane and is released to the culture medium. The particles within the cell can be obtained by three freeze-thaw cycles. Foamy virus virion formation occurs only in the presence of its envelope. The foamy virus, therefore, cannot be pseudotyped with the VSV-G envelope protein in order to concentrate the vector by centrifugation, as demonstrated for other retroviral vector systems. However, the foamy virus can be concentrated to more than a 100fold without loss of infectivity. Therefore, if needed, SFV-1 vector can be concentrated by centrifugal ultrafiltration (Centricon, Amicon).

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23 Recombinant Feline Immunodeficiency Virus Vectors Preparation and Use Michael A. Curran and Garry P. Nolan

1. Introduction Traditional onco-retroviral vector packaging systems, typified by those based on Moloney murine leukemia virus (MMLV), have many appealing features for gene transfer. MMLV vectors stably integrate their genome into their target cells, can package and carry up to 6.5 kb of foreign insert, can be produced free of helper virus, and, because of their low immunogenicity, can be administered in vivo multiple times to the same organism. The major disadvantage of these vectors; however, is their inability to transduce nondividing cells (1). Lentiviral packaging systems, such as those based on the human and feline immunodeficiency viruses (HIV and FIV), possess all the strengths of the oncoretroviral systems coupled to the ability to transduce most nondividing and primary cells. This chapter focuses on the preparation and optional concentration of FIV vector particles, as well as on transduction of target cells with these viral preparations. Before moving on to the practical methods of FIV production, it is useful to begin with an understanding of FIV biology, particularly the elements of the virus that allow infection of nondividing cells. Although most cell types are susceptible to transduction with FIV vectors, there are a few known exceptions, which are also discussed. More thorough reviews of the biology of lentiviruses and lentiviral vectors can be found in the literature (2,3).


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Fig. 1. FIV genome and vector systems. (A) The 9.4-kb FIV genome showing all ORFs and the protein constituents of the Gag-Pol polyprotein. (B) Second- and thirdgeneration FIV-based FELIX vectors. Shown are a reporter transfer vector, the packaging vector, and a VSV-G envelope vector for both three-plasmid systems. (C) Schematic depicting the production of recombinant FIV for gene transfer using one of the triple transient transfection systems shown above.


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1.1. FIV Genomic Organization and Life Cycle The genomes of the simple (i.e., non-lenti, non-spuma) retroviruses contain three genes coding for the Gag, Pol, and Env proteins, which encode the structural, enzymatic, and surface proteins, respectively. In addition to these essential open reading frames (ORFs), lentiviral genomes typically contain several accessory genes that perform complex functions in both the production and infection stages of their life cycle. Within its 9.4-kb genome, FIV possesses three accessory genes, vif (increases infectivity of virus produced in lymphocytes), ORFA/ORF2 (weak LTR transactivator), and rev (facilitates nucleocytoplasmic transport of intron-containing viral RNA), which encode proteins important in the viral life cycle (4) (Fig. 1A). Third-generation vector systems that eliminate these accessory proteins for the sake of added safety must, to some degree, compensate for their functions in virus production or suffer losses in infectious viral titer. The FIV life cycle begins with transcription of the viral genome from the U3 promoter region of the 5' long terminal repeat (LTR), so named because it is present in tandem at both ends of the retroviral genome. Full-length transcripts are terminated and polyadenylated at the U5 region of the 3' LTR. Completely spliced variants of this transcript give rise to the Rev and A proteins. Rev then returns to the nucleus, binds to the Rev responsive element (RRE) present at the 3' end of the env gene, and promotes nuclear export of partially spliced and unspliced viral RNA. Partially spliced transcripts give rise to the Vif and Env proteins, and unspliced transcripts yield the Gag and Gag-Pol (generated through ribosomal frameshifting) polyproteins and also serve as the genome for packaging into mature virions. The viral protease cleaves itself away from Gag-Pol and then processes Gag into matrix (MA), capsid (CA), and nucleocapsid (NC), and Pol into integrase (IN), reverse transcriptase (RT), and a dUTPase. Upon entering a target cell (notably via CXCR4 or CCR5), the FIV genome is reverse transcribed into double-stranded DNA by RT and transported to the nucleus in the context of the preintegration complex (MA, IN, RT), where it is integrated into the host cell genome. The ability to transduce nondividing cells can probably be attributed to several features of FIV. Although specific NLS cites have not been mapped for FIV as precisely as they have for HIV, it is possible that FIV contains sequences in its MA and IN proteins that facilitate its entry into the nucleus via a karyopherin-mediated pathway analogous to HIV (5,6). Also, by analogy to HIV and equine infectius anemia virus (EIAV), FIV probably also contains a central DNA flap region that facilitates its entry into the nucleus through an unknown mechanism (7). Interestingly, FIV contains a dUTPase as part of its Pol polyprotein that is not present in HIV Pol. Mutation studies of the FIV and

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EIAV dUTPases suggest that their function is to proofread the viral genome for uracil mis-incorporations, which can occur more frequently in metabolically inactive cells with low nucleotide pools (8,9). Thus, the ability of FIV to infect nondividing cells efficiently in vivo probably results from the synergy of several viral components acting at multiple stages of the viral life cycle. 1.2. Development of FIV Vectors Although the three labs responsible for developing FIV-based vector systems have taken slightly different approaches, most key steps in adapting FIV into a useful vector system are common to all three systems (10–12). In all systems, a transfer vector (carries the gene of interest), a packaging vector (produces the FIV structural proteins), and an envelope vector (directs virion entry through binding to a cognate receptor on target cells) are transfected together into human 293T-cells to produce virus. Viral supernatants are collected 48 h posttransfection and added to target cells to allow infection by the vector particles present in the supernatants. All FIV, and almost all retroviral, production systems use 293T cells as their packaging cells (i.e., the cells in which virus is produced) because of their high transfectability, parental species (i.e., human), and strong metabolic activity. The native FIV U3 promoter, however, exhibits very low activity in human cells, resulting in very little viral genome transcription following transfection into 293T cells (13). For this reason, all FIV vectors contain the human cytomegalovirus (hCMV) enhancer/promoter, which is very strong in 293T cells, grafted in place of the native FIV U3 promoter. Since this hCMV promoter is present only in the 5' LTR of the vector, integrated FIV vector genomes will contain the native viral LTR at both the 5' and 3' ends of the genome (the 3' U3 region serves as the template for both LTRs during reverse transcription). This again creates a transcription problem, necessitating the use of an internal promoter to drive expression of the gene(s) of interest. The upstream hCMV promoter modification and insertion of an internal promoter are common transcriptional modifications necessary to make FIV viable as a vector. Like the onco-retroviral vector systems, FIV packaging systems require expression of the viral Gag-Pol protein and an envelope protein (e.g., MMLV amphotropic, vesicular stomatitis virus G [VSV-G]) in order to produce infectious particles. Of the FIV accessory proteins, Vif is not needed by virtue of using 293T cells as producers, and replacement of the FIV U3 promoter with CMV makes A dispensable; however, all FIV vectors excluding the third-generation Nolan lab vectors require the viral Rev protein for efficient nuclear export of unspliced vector genome. In general, second-generation FIV packaging vectors produce some or all of the viral accessory proteins, whereas thirdgeneration packaging constructs produce only Gag-Pol.


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Fig. 2. Second-generation FIV transfer vectors for cloning. Shown are maps of the pFLX-CPL series of vector, which contain only a multiple cloning site (MCS), the pFLX-CRS vector, which contains a promoter upstream of the MCS, and pFLXCRSIG, which contains an IRES-eGFP cassette downstream of a promoter and MCS.

1.3. Second-Generation FIV Vectors All second-generation FIV vector systems are based on transient triple transfection of a transfer vector, packaging vector, and envelope construct into 293T-cells. There are currently no stable FIV packaging cell lines. All vector names used in the remainder of the text refer to the FELIX system developed in the Nolan lab. From a practical point of view, the transfer vector is the most interesting, as it will carry the gene of interest to the target cell and control its expression following integration into the genome. As mentioned above, all FIV transfer vectors contain the hCMV promoter cloned upstream of the 5' regions necessary for replication and packaging (i.e., R, U5, and the packaging signal) (Fig. 1B). Optimal packaging of FIV vectors requires a region that extends into the Gag reading frame; consequently, most vectors include an FIV

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sequence up to the MfeI (+875 bp into the provirus) site or maximally to the TthIII1 site (+921 bp). This large packaging region includes the major 5' splice donor as well as the Gag ATG, which have not been removed in most vectors currently available. The 3' end of all transfer vectors includes the 3' end of the env gene (which includes the RRE) and the complete 3' LTR. The gene cassette of interest is inserted between the packaging region and the 3' region (RRE and LTR) described above. Positive control vectors such as pFLX-RSG contain a central Rous sarcoma virus (RSV) promoter driving expression of the green fluorescent protein (GFP). For most applications, the vectors pFLX-CPL or pFLX-CRS are used as backbones into which a particular gene or gene cassette of interest is inserted (Fig. 2). pFLX-CPL contains the multiple cloning site (MCS) from pBluescript II inserted in one of two orientations (KS or SK)—this vector is designed for cloning in promoter-gene combinations of interest, allowing them to be transferred over easily from standard plasmids or MMLV vectors using internal promoters. pFLX-CRS contains an RSV promoter upstream of the MCS from pBluescript in the KS orientation and is designed for cloning of cDNA inserts. A variant of pFLX-CRS that contains an internal ribosome entry site (IRES)-GFP marker cassette downstream of the MCS, pFLX-CRSIG, is also available. The transfer vector is cotransfected into 293T-cells along with the packaging vector and envelope vector. The second-generation packaging vectors available—pCPRdEnv and pCFWdEnv—both contain a CMV promoter driving expression of all the FIV proteins except Env. They have been rendered packaging deficient by deletion of the entire LTR and packaging region up to 500 bp into the proviral genome. In pCPRdEnv, the Env protein has been neutralized by introduction of a point mutation early in the reading frame that truncates and frameshifts the protein, whereas in pCFWdEnv there is a deletion in env that removes part of the ORF and frameshifts the remainder. pCPRdEnv is derived from the PPR strain of FIV, whereas pCFWdEnv is derived from the 34TF10 strain. In general, pCPRdEnv and pCFWdEnv give approximately equivalent titers when used with the transfer vectors described above (all of which are based on FIV-34TF10). FIV vectors can be pseudotyped with several amphotropic/polytropic envelopes, yielding high titres and broad host range. The best titers for all FIV vector system are achieved by using the glycoprotein VSV-G as the envelope protein (14). In the FELIX system, this envelope is expressed off the CMV promoter on the pCI-VSVG plasmid. VSV-G pseudotyped virions can enter almost all eukaryotic cells (from Drosophila to human) and can be concentrated using high-speed centrifugation. FIV vectors also pseudotype effectively with the MMLV amphotropic envelope. In contrast, FIV vectors do not pseudotype well with the MMLV ecotropic envelope or with the Gibbon-Ape leukemia virus (GALV) envelope.


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In summary, triple transfection of an FIV transfer vector (e.g., pFLX-RSG), a packaging vector (e.g., pCPRdEnv), and a VSV-G envelope vector (e.g., pCIVSVG) into 293T-cells yields viral titers in the 106 IU/mL range. The particles can be used to transduce a wide variety of dividing and nondividing target cells permanently with the gene of interest carried in the transfer vector. 1.4. Third-Generation FIV Vectors The second-generation FIV vectors yield good viral titres and are very useful for in vitro work and in vivo work in animal models. The potential for use of FIV vectors in human subjects, however, encouraged the creation of a system in which the packaging and transfer vectors contained less native FIV sequence and in which no viral accessory proteins were present during the packaging or transduction phases of the vector life cycle (Fig. 1B). The most significant changes in the third-generation system are in the packaging vector. pRSV-FIVGP, the third-generation packaging construct, expresses only the viral Gag-Pol protein with a linked Lyt2 surface marker. Since Gag-Pol contains splice donors, an RNA element known as the cytoplasmic transport element (CTE) has been included to facilitate nuclear export of intact Gag-Pol-IRES-Lyt2 mRNA. The CTE is a structured RNA element from Mason Pfizer monkey virus (MPMV, a type D retrovirus) that functions like the Rev-RRE systems of the lentiviruses, but without the need for a cognate Rev protein (15). The third-generation transfer vectors, typified by the LacZ reporter vector pFLX-YCL, contain a CTE in place of the FIV RRE to facilitate their nucleocytoplasmic transport. Interestingly, the CTE must be placed as far 3' as possible in the vector to provide efficienct nuclear export. As the third-generation vectors are rarely used for in vitro work or animal studies, no transfer vectors with convenient MCSes exist as of this writing. Titers of the third-generation system (e.g., pFLX-YCL, pRSV-FIVGP, pCI-VSVG) are in the 106 IU/mL range but are generally between 1.5-fold and 2-fold less than those of the second-generation system, reflecting the lack of efficiency of the CTE relative to the FIV Rev-RRE system. 1.5. FIV Vector Tropism When they are pseudotyped with the VSV-G envelope, it is believed that FIV vector particles can enter almost any target cell type. In in vitro systems, FIV vectors infect G1/S- and G2/M- arrested cells with efficiencies similar to infection of dividing cells (10,12). Primary cells transduced by FIV vectors include human aortic smooth muscle cells, human umbilical vein endothelial cells, human hepatocytes, human CD34+ progenitor cells, human T-cells, human dendritic cells, human pancreatic islet cells, stimulated murine T-cells,

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rat neurons, and rat pancreatic islet cells. In our hands, however, murine hematopoeitic progenitor cells and completely unstimulated (no cytokines or antibodies) human T-cells have yielded no significant transduction with FIV vectors. Also, FIV (and HIV) vectors seem to have a quantitative defect for infecting some murine (specifically murine, not rat) cells as titers measured for these vectors on some human cells fall off between 2- and 10-fold on similar murine cells. This defect may be even more pronounced on murine primary cells, but more work needs to be done to confirm this phenomenon. See www.stanford.edu/group/Nolan for updates. 2. Materials 2.1. Cell Culture 1. Human embryonic kidney 293T-cells. Cells should be grown in the DMEM described below and should be split 1/5 to 1/10 every 3–4 days. 2. Dulbecco’s modified Eagle’s medium (DMEM) with high glucose, L-glutamine, 110 mg/L sodium pyruvate, and pyridoxine hydrochloride (Gibco-BRL, cat. no. 11995-065). Optionally, supplement with penicillin-streptomycin (Gibco-BRL, cat. no. 15140-122) or with penicillin-streptomycin-amphotericin B (Gibco-BRL, cat. no. 15240-062). 3. Trypsin-EDTA solution 1× (Gibco-BRL, cat. no. 25300-054). 4. Fetal bovine/calf serum (FBS/FCS). 5. Tissue culture treated dishes (6 or 15 cm diameter).

2.2. Transfection Reagents 2.2.1. Ca3(PO4)2 Transfection 1. 2. 3. 4.

Chloroquine: Stock is 50 mM in ddH2O (Sigma, cat. no. C-6628). CaC12: Stock is 2 M in ddH2O, 2-μm filtered (Mallinkrodt, cat no. 4160). HEPES sodium salt (Sigma, cat no. H-7006). Na2HPO4 dibasic (Fisher, cat no. S374-500). Stock solution is 5.25 g dissolved in 500 mL ddH2O (i.e., approx 74 mM). 5. 2× HBS: 8.0 g NaCl, 6.5 g HEPES, 10 mL Na2HPO4 stock solution. pH to 7.0 using NaOH or HCl. Bring volume up to 500 mL. Check pH again. The pH is very important; it must be exactly 7.0.

2.2.2. FugENE 6 Transfection 1. FuGENE 6 Transfection Reagent (Roche, cat no. 1 814 443). 2. Opti-MEM (Gibco-BRL, cat. no. 31985-070).

2.4. FIV Vector Plasmids 1. An FIV transfer vector containing a reporter gene cassette or promoter and gene of interest to be transferred to a target cell (e.g., pFLX-RSG). DNA should be prepared using a large-scale plasmid purification method that yields pure plasmid DNA and minimal endotoxin.


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2. An FIV packaging plasmid vector (e.g., pCPRdEnv). DNA should be prepared as above. 3. A plasmid expressing an envelope with which FIV vectors readily pseudotype (e.g., pCI-VSVG). DNA should be prepared as above.

2.5. Virus Purification 1, 5-mL syringes. 2. 0.45-μm low-protein-binding syringe filters. 3. 15-mL sterile polypropylene tubes.

2.6. Virus Concentration 1. Tris-NaCl-EDTA buffer (TNE): 50 mM Tris-HCl, pH 7.8, 130 mM NaCl, 1 mM EDTA. Add 50 mL of 1 M Tris-HCl, pH 7.8, to 950 mL H2O containing 7.6 g of NaCl, 0.4 g of EDTA and autoclave prior to storage at 4°C. 2. 50 mL Oak Ridge polyproylene copolymer tubes (Nalgene Nunc, cat. no. 31390050). 3. 0.45-μm low-protein-binding 115 mL Nalgene filters (cat. no. 245-0045).

2.7. Infection Reagents 1. Polybrene (hexadimethrine bromide, Sigma, cat. no. H9268). 1000× stock concentration is 5 mg/mL in PBS. 2. Retronectin (Panvera, cat. no. TAK T100).

3. Methods 3.1. Production of Recombinant Virus Described below are the two methods for triple transfection of 293T-cells that have worked the best and most reproducibly in our experience. In each case, 293T-cells are transfected with 5 μg of packaging vector plasmid, 3 μg of transfer vector plasmid, and 2 μg of envelope vector plasmid; 48 h later, recombinant FIV viral supernatants are collected from these cells. Both the transfection methods described below and the ratio of packaging to transfer to envelope vector are open to further optimization. Conditions described below are for 6cm dishes; however, larger or smaller dishes may be used providing all the DNA and reagent volumes are scaled appropriately based on the difference in surface area. The FuGENE 6 protocol is recommended for its consistently high yields and low toxicity; however, calcium phosphate transfection provides a much more economical alternative. Note that 33% infected, some cells will have multiple integration events. 1. Prepare viral supernatants using a transfer vector expressing a reporter gene that can be detected by fluorescence-activated cell sorting (FACS; i.e., GFP, β-Gal, or a surface marker that can be detected by an antibody). 2. Split 1 × 105 cells/well of a 12-well plate of the cell line to be used for measuring titer. For each sample to be titered, split out three wells. The ideal is for there to be approximately 1 × 105 cells/well at the time of infection; thus, if you are splitting the day before, you may want to seed 5 x 104 cells/well. 3. To the three wells allocated for each sample, add 100 μL of viral supernatant + 900 μL media to one, 500 μL virus + 500 μL media to the other, and 1 mL of virus to the last (see Note 11). 4. Add 1 μL of 1000× Polybrene to each well. 5. Spin plates for 1.5 h at 2500 rpm. 6. Incubate plates for 8–16 h at 32°C.

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7. Remove virus and add fresh media. 8. Incubate plates for 36–48 h at 37°C. 9. Measure the percentage of cells infected by FACS analysis (e.g., on a BD FACScan). 10. Calculate titer for all three wells individually as follows: Well #1: %infected × 1 × 105 × 10 × 10 = titer IU/mL Well #2: %infected × 1 × 105 × 2 × 2 = titer IU/mL Well #3: %infected × 1 × 105 × 1 × 1 = titer IU/mL. The general method is %infected × no. of cells infected × fraction of 1 mL of virus used × final dilution in media. 11. Average all three titers to get a working titer. If virus volume is limiting, preparing and analyzing only the 100- and 500-μL wells still gives a good titer estimate.

4. Notes 1. 293T cells may be selected with 1 mg/mL G418 if they begin to lose their transfectability or if their growth rate slows. 2. The chloroquine is toxic to the 293T cells, limiting transfection time to 8 h. If longer incubation times are necessary, less chloroquine can be used. 3. Because of their repeated LTRs and large size, some FIV vectors may be more stable when prepared in stable bacterial strains such as SURE (Stratagene) or STBL2 (Gibco). 4. After applying the HBS/DNA mixture, a fine granular black precipitate should be visible above the cell monolayer. (This will become more pronounced throughout the 8 h.) Less fine precipitates with larger black particles can signal suboptimal transfection and greater toxicity. 5. Recombinant virus is more stable at 32°C; therefore, incubation of plates at 32°C prior to and/or during virus collection(s) may yield higher titers than incubation at 37°C. 6. For FuGENE transfections, in general, use 2.67 μL FuGENE 6/1 μg of DNA. 7. Filtration removes any remaining cell debris and helps reduce carry-over transfection when it is a problem. 8. Flash-freezing supernatants on dry-ice/ethanol or in liquid nitrogen provides the best viability. Alternatively, supernatants can be placed directly at –80°C. 9. Lower concentrations of serum are used when concentrating viral supernatants so that fewer precipitated serum proteins pellet with the virus particles. 10. Skipping filtration yields highest titers; however, unfiltered concentrated virus may be toxic to cells owing to residual VSV-G coated membrane fragments. 11. Concentrated virus may be toxic to some cells because of the fusogenic nature of VSV-G pseudotyped particles. It is recommended that the concentrated virus first be applied to the target cells in a variety of dilutions to establish an optimal range of transduction to toxicity. 12. Addition of media to the TNE/virus solution helps make the virus preparation less toxic for certain primary cells and provides additional liquid volume for resuspension.


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13. Addition of polycationic molecules such as Polybrene is known to enhance retroviral transduction; however, little evidence exists that this effect is additive when using recombinant fibronectin. 14. Spin infection is known to enhance retroviral transduction; however, little evidence exists that this effect is additive when using recombinant fibronectin.

References 1. Miller, D. G., Adam, M. A., and Miller, A. D. (1990) Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection [published erratum appears in Mol. Cell. Biol. 1992: 433. Mol. Cell. Biol. 10, 4239–4242. 2. Naldini, L. (1998) Lentiviruses as gene transfer agents for delivery to non-dividing cells. Curr. Opin. Biotechnol. 9, 457–463. 3. Trono, D. (2000) Lentiviral vectors: turning a deadly foe into a therapeutic agent. Gene Ther. 7, 20–23. 4. Tomonaga, K. and Mikami, T. (1996) Molecular biology of the feline immunodeficiency virus auxiliary genes. J. Gen. Virol. 77, 1611–1121. 5. Bukrinsky, M. I., Sharova, N., Dempsey, M. P., et al. (1992) Active nuclear import of human immunodeficiency virus type 1 preintegration complexes. Proc. Natl. Acad. Sci. USA 89, 6580–6584. 6. Gallay, P., Stitt, V., Mundy, C., Oettinger, M., and Trono, D. (1996) Role of the karyopherin pathway in human immunodeficiency virus type 1 nuclear import. J. Virol. 70, 1027–1032. 7. Zennou, V., Petit, C., Guetard, D., et al. (2000) HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 101, 173–185. 8. Lerner, D. L., Wagaman, P. C., Phillips, T. R., et al. (1995) Increased mutation frequency of feline immunodeficiency virus lacking functional deoxyuridinetriphosphatase. Proc. Natl. Acad. Sci. USA 92, 7480–7484. 9. Lichtenstein, D. L., Rushlow, K. E., Cook, R. F., et al. (1995) Replication in vitro and in vivo of an equine infectious anemia virus mutant deficient in dUTPase activity. J. Virol. 69, 2881–2888. 10. Curran, M. A., Kaiser, S. M., Achacoso, P. L., and Nolan, G. P. (2000) Efficient transduction of non-dividing cells by optimized feline immunodeficiency virus vectors. Mol. Ther. 1, 31–38. 11. Poeschla, E. M., Wong-Staal, F., and Looney, D. J. (1998) Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors. Nat. Med. 4, 354–357. 12. Johnston, J. C., Gasmi, M., Lim, L. E., et al. (1999) Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. J. Virol. 73, 4991–5000. 13. Miyazawa, T., Kawaguchi, Y., Kohmoto, M., Tomonaga, K., and Mikami, T. (1994) Comparative functional analysis of the various lentivirus long terminal repeats in human colon carcinoma cell line (SW480 cells) and feline renal cell line (CRFK cells). J. Vete. Med. Sci. 56, 895–899.

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14. Burns, J. C., Friedmann, T., Driever, W., Burrascano, M., and Yee, J. K. (1993) Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells [see comments]. Proc. Nat.l Acad. Sci. USA 90, 8033–8037. 15. Bray, M., Prasad, S., Dubay, J. W., et al. (1994) A small element from the MasonPfizer monkey virus genome makes human immunodeficiency virus type 1 expression and replication Rev-independent. Proc. Nat.l Acad. Sci. USA 91, 1256– 1260.

A SIV-Based Lentivirus Vector

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24 Lentivirus Vector Based on Simian Immunodeficiency Virus Development and Use Klaus Überla

1. Introduction Vector systems based on human immunodeficiency viruses (HIVs) (1) allow an efficient and stable gene transfer into nondividing cells (2,3). Because of the pathogenicity of the parental virus, the use of lentiviral vectors based on feline immunodeficiency virus (4,5), equine infectious anemia virus (6), or simian immunodeficiency virus (SIV) (7,8) has also been explored. SIV is closely related to HIV, and some strains of SIV can induce an AIDS-like disease in nonhuman primates. This animal model has been extensively used to study the pathogenesis of immunodeficiency virus infections and should also be valuable for a preclinical safety assessment of SIV-based vectors. Although SIV can replicate in human CD4+ cells, the course of laboratory-acquired infections suggests greatly reduced virulence in comparison with HIV (9). The aim of this chapter is to discuss various practical aspects of the development and use of SIV-based vectors. This is preceded by a short overview of the genome structure and replication cycle of the virus. More detailed information on the molecular biology of immunodeficiency viruses can be obtained from recent reviews (10,11). 1.1. Genome Structure The viral genome is flanked by two long terminal repeats (LTRs; Fig. 1A), which consist of U3, R, and U5 regions. The U3 region harbors the promoter From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Map of proviral DNA and mRNA transcripts of SIV (A) and maps of SIV vector and packaging constructs (B). Deleted regions are shaded. Inactivated reading frames are marked in black. Hatched regions indicate codon optimization. ψ, assumed packaging signal; CMV, immediate early promoter and enhancer of human cytomegalovirus; polyA, heterologous polyadenylation signal; Prom, heterologous promoter; GFP, gene for the green fluorescence protein. Plasmids Sgpsyn (13), Hgpsyn (13), pcTat (16), pcRev (17), and pHIT-G (20) have been previously described.


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and enhancer elements, which direct initiation of viral transcription at the 5'LTR. All viral transcripts start with the 5'R region and end with the 3'R region. Differential splicing and ribosomal frameshifting allow expression of various open reading frames. Five of them (gag, pol, env, tat, and rev) are particularly relevant for vector development. The gag reading frame codes for the matrix and capsid proteins, pol for viral enzymes, and env for the surface protein. TAT is a strong transcriptional activator; it binds to the trans-acting responsive region, TAR, at the 5'end of the viral RNA. Rev also binds to a secondary structure of the viral RNA, called Rev-responsive element (RRE), and mediates nuclear export of unspliced or singly spliced viral RNA. 1.2. Replication Cycle The viral particle, which contains two copies of the unspliced viral RNA, binds via the Env protein to the cellular receptors, leading to fusion of the viral and cellular membrane. This delivers the viral core to the cytoplasm, where the core dissociates. The viral RNA is reverse transcribed by the particle-associated reverse transcriptase. During reverse transcription the 5'U5 and 3'U3 regions of the viral RNA serve as templates for the 3'U5 and 5'U3 regions, respectively. This ensures regeneration of two complete LTRs during DNA synthesis. After transport of the viral DNA into the nucleus, it integrates into the genome of the cell with the help of the viral integrase. The viral genome is then transcribed by cellular factors. During the early phase of the viral life cycle, multiply spliced transcripts coding for Tat and Rev are formed. Tat acts as a strong activator of viral transcription, leading to a positive feedback loop. If sufficient amounts of Rev have accumulated, Rev mediates export of unspliced and singly spliced transcripts to the cytoplasm, where they are translated into Gag, Gag-Pol, and Env. The viral particle then assembles at the plasma membrane. RNA secondary structures presumably located at the 5' untranslated region and in the beginning of gag act as packaging signals, leading to the incorporation of two copies of unspliced viral RNA into the particle. Finally, the viral particle buds off the membrane, leading to the release of infectious virus particles. 1.3. Development of SIV-Based Vectors The key step in the development of lentiviral vectors is to split up the viral genome in three or more constructs, which will provide all functions necessary for a single round of infection. Usually, two packaging constructs are used: one codes for the surface protein (pHIT-G, Fig. 1B), and the second allows expression of gag and gag-pol (SgpΔ2frx or Sgpsyn, Fig. 1B). Both of them lack packaging signals and elements required for reverse transcription and integration. Therefore, cotransfection of both packaging constructs leads to the

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production of empty particles, which cannot transfer either env, gag, or gagpol. If the packaging constructs are cotransfected with a vector construct (ViGΔSB, Fig. 1B), the encoded vector RNA can be packaged and transferred. The features of these three constructs are discussed separately in more detail below. 1.3.1. Selection of the Envelope Protein The envelope protein (Env) of the vector particle is an important determinant of cell tropism. In the case of SIV-based vectors, the homologous Env protein would only provide entry into CD4+ cells, which also express the right coreceptor. Since heterologous cell surface proteins can also be incorporated into lentiviral vector particles, the SIV Env can be replaced by heterologous envelope proteins such as the amphotropic murine leukemia virus (MLV) Env or the G-protein of vesicular stomatitis virus (VSV-G) (7). Both allow entry into a wide variety of different cells. The VSV-G has the additional advantage that its stable association with the vector particle allows purification and concentration (12). The toxicity of VSV-G makes the establishment of stable packaging cell lines difficult. Toxic effects can also be observed at high doses on some target cells and might limit its application in vivo. 1.3.2. Minimizing the Vector Construct Since the vector RNA encoded by the vector construct is transfered to target cells, it is desirable to eliminate as many viral sequences as possible. cis-acting sequences that cannot be deleted from the vector construct are promoter and enhancer elements in the 5'LTR, the packaging signal (ψ), and elements required for reverse transcription or integration such as the primer binding site, the 3' polypurine tract, the R regions, and the ends of the LTRs. Most vector constructs also require the RRE, since 5'gag sequences, which were included for better packaging, render the constructs Rev dependent (ViGΔSB, Fig. 1B). One exception is a minimal vector construct that only contains viral sequences present on the multiply spliced nef transcript (7). The vector titers of this RREless vector are, however, approximately 10-fold lower than titers of vectors containing 5'gag sequences. Deletion of the promoter and enhancer elements of the U3 region of the 3'LTR leads to self-inactivating vectors, which have a reduced risk of vector mobilization by superinfection of transduced cells with HIV. The deletion in the 3'U3 region does not affect transcription of vector RNA in the vector producer cells since transcription is controlled by the 5'U3 region. During reverse transcription the 3'U3 region serves as a template for the 5'U3 region of the viral DNA in the target cells. If the promoter and enhancer elements of the 3'U3 region have been deleted, the 5'U3 region will also lack these elements in the target cells. Therefore, the packaging signals


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present in the 5'untranslated regions are no longer transcribed in the target cells, reducing the risk of vector mobilization by superinfection of transduced cells with HIV. Insertion of an internal promoter upstream of the therapeutic gene allows its expression in the target cells and offers the possibility of transcriptional targeting (ViGΔSB, Fig. 1B). Problems of promoter interference in target cells can also be circumvented by these self-inactivating vectors. When different therapeutic genes are cloned into the same vector construct, the titers can vary considerably. Although the reasons for failures are not always understood, the following points should be considered when designing new vector constructs. The overall length of the vector should be kept as short as possible. It is recommended that the vector construct not exceed the length of the wild-type SIV genome, which is roughly 10 kb. The therapeutic gene is usually inserted in the sense orientation to avoid antisense inhibition phenomena during vector production. Polyadenylation signals must be absent, and elimination of cryptic splice sites can signficantly increase the titer of some vectors. Direct repeats should also be avoided, since strand transfer during reverse transcription can lead to the deletion of intervening sequences. If the therapeutic gene is to be inserted in the antisense orientation, it is advisable to use an internal promoter that has low activity in the vector producer cells. 1.3.3. Optimizing the gag-pol Expression Plasmid The most efficient SIV gag-pol plasmids had initially preserved the functional organization of the SIV genome (7). Sequences involved in packaging were deleted from the 5'untranslated region (SgpΔ2frx, Fig. 1B). The 3'LTR had been replaced by a heterologous polyadenylation signal. Deletions were also introduced into the env gene and the accessory genes vif, vpr, vpx, and nef. The Tat-TAR transcriptional activation pathway and the Rev-RRE nuclear export system had been left untouched for efficient expression of gag-pol. One of the disadvantages of such gag-pol expression plasmids is that the gag-pol genes are flanked by two regions that are homologous to vector sequences. These regions of homology are gag sequences, which are maintained on the vector for better packaging, and the RRE, which is required on most SIV vector constructs for export of the unspliced vector RNA from the nucleus to the cytoplasm. Homologous recombination events between the gagpol expression plasmid and the vector could therefore lead to transfer of gagpol sequences into target cells. The risk for these homologous recombination events was limited by optimizing the codon usage of SIV gag-pol (13) without changing the amino acid sequence. The degree of nucleotide sequence identity to gag sequences present on the vector construct was thus reduced to 75%. The degree of homology between vector and gag-pol expression plasmid could be

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further minimized by packaging the SIV vector with a codon-optimized HIV-1 gag-pol expression plasmid (13). As observed previously, optimization of lentiviral codon usage (14,15) also allowed Rev-independent expression of gag-pol. Therefore the RRE could also be omitted from the codon-optimized gag-pol expression plasmids, which finally only contain the gag-pol open reading frame without any other lentivirus-derived sequences. When the codonoptimized gag-pol expression plasmid is used to package vector constructs such as ViGΔSB, tat and rev expression plasmids (pcTat, pcRev [16,17]) are cotransfected for efficient transcription and nuclear export of the vector RNA, respectively. 2. Materials 2.1. Cell Culture 1. Cell culture medium: Dulbecco’s modified Eagle’s medium (DMEM)-Glutamax (Gibco-BRL cat. no. 61965-026, Life Technologies, Karlsruhe, Germany) + 100 U penicillin G/mL + 100 μg streptomycin/mL. 2. 293T cells (293ts/A1609 [18]) are cultured in DMEM + 10% fetal bovine serum (FBS). Cells are split 1/10 twice a week by trypsin-EDTA (Gibco-BRL cat. no. 25300-054, Life Technologies) treatment. Overgrowth should be avoided. Thaw fresh cells every 3–4 months. 3. 293A cells (Quantum Biotechnologies, Montreal, Canada) kept in DMEM + 5% FBS are split 1/5 twice a week.

2.2. Plasmids The Qiagen (Hilden, Germany) Plasmid Mini Kit (cat. no. 12143) or the EndoFree Plasmid Maxi Kit (cat. no. 12362) are used to prepare plasmid DNA of the packaging and the vector constructs (Fig. 1B and see Note 1). 2.3. Generation of Vector Particles by Transient Transfection 1. 2× HBS: 10× solution: 8.18% NaCl, 5.94% Hepes, 0.2% Na2HPO4 (all w/v). Dilute to 2× HBS solution. Add 1 M NaOH to bring pH to 7.12. Filter-sterilize and store in aliquots at –20°C. 2 M CaCl2. 2. Injectable water (B. Braun, Melsungen, Germany). 3. Carrier DNA: Sonicated calf thymus DNA (Gibco-BRL cat. no. 15633-019, Life Technologies). 4. 0.45 μm filter: Minisart (Sartorius cat. no. 17598K, Göttingen, Germany).

2.4. Concentration of Vector Supernatants 1. Serum-free medium: AIM-V medium (Gibco-BRL cat. no. 12055-083, Life Technologies). 2. Vivaspin 20 tubes (Sartorius cat. no. VS2041).


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3. Methods 3.1. Generation of Vector Particles by Transient Transfection Vector particles are prepared by transient cotransfection of the packaging constructs with the vector construct into 293T cells using the calcium phosphate coprecipitation method since stable packaging cell lines for SIV-based vectors are not yet available (see Note 2). 1. On the day prior to transfection plate 1 × 106 293T cells in 25-cm2 tissue culture plates in 5 mL DMEM + 10% FBS, which should give about 80% confluency on the next day. 2. Replace the culture medium with fresh prewarmed (37°C) medium and incubate for 4–6 h at 37°C and 5% CO2 (see Notes 3 and 4). 3. To set up the transfection cocktail, thaw all reagents at 37°C and place on ice. 4. Mix on ice 5 μg gag-pol expression plasmid, 2 μg VSV-G expression plasmid, and 5 μg vector plasmid with carrier DNA to a total amount of 15–20 μg DNA. 5. Add 31 μl 2 M CaCl2 to the DNA and adjust the volume to 250 μl by adding injectable water. 6. For each tissue flask to be transfected, aliquot 250 μl 2 × HBS into a separate 1.5mL reaction tube. 7. Place one tube at a time on a vortexer under the tissue culture hood and add the DNA-CaCl2 solution drop by drop. 8. After a 10-min incubation period at room temperature, pipet the transfection cocktail into the medium of the 293T cell flasks, mix by gentle rocking, and place in the incubator. 9. Eighteen to 24 h after addition of the transfection cocktail, replace the medium gently with 5 mL fresh culture medium. 10. One and/or 2 days later, remove the supernatant of the transfected cells and clear by low-speed centrifugation (370g, 10 min). 11. Then slowly press the supernatant with a syringe through 0.45-μm filters and store in aliquots at –80°C. Filtered supernatants can be stored at 4°C, if infections are set up within a day after harvest (see Note 5).

3.2. Titration of Vectors The titers of vectors expressing the green fluorescence protein (GFP) reporter gene are determined as follows. 1. One day prior to infection plate 5 × 104 293A cells in 1 mL DMEM + 5% FBS per well of a 24-well plate (see Note 6). 2. Thaw vector stocks briefly at 37°C and make 10-fold serial dilutions in DMEM + 5% FBS. 3. Remove the medium from the wells of the 24-well plate and add 200 μL of vector dilutions immediately. 4. After 4 h in the CO2 incubator, add 1 mL prewarmed DMEM.

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5. Two to 3 days later, count the number of GFP+ cells in an inverted fluorescence microscope. 6. To calculate the titer without having to view the entire well, first count the number of optical fields at a given magnification that can be fitted across the diameter of the well. 7. Then determine the average number of GFP+ cells per optical field at this magnification from a representative number of optical fields. 8. Multiply the number of GFP+ cells per optical field by the square of the number of optical fields fitting the diameter of the well, to give the number of GFP+ cells per well. 9. Multiplication by 5 and by the dilution factor gives the number of GFP-forming units per mL vector supernatant.

3.3. Concentration of Vectors Vector supernatants can be easily concentrated approximately 100-fold by filtration through Vivaspin 20 tubes if the supernatants were harvested in serum-free medium. This is achieved as follows: 1. Replace the DMEM medium 24 h after addition of the transfection cocktail with the same volume of serum-free AIM-V medium. 2. Than harvest supernatants 24 and 48 h later and clear and filter as described in Subheading 3.1. 3. Sterilize the Vivaspin columns by washing with 70% ethanol and subsequent drying in the cell culture hood. 4. Add 20 mL of cleared and filtered vector supernatant to the upper chamber of the Vivaspin 20 tube and centrifuge at 2800g for 2 h. 5. Measure the volume of the remaining fluid with a 200-μL pipet. 6. If the volume is larger than 200 μL, continue centrifugation. 7. Once the desired concentration factor has been reached, the concentrated supernatant can be frozen in aliquots and titered as described in Subheading 3.2. The recovery rate is usually >90% (see Note 7).

4. Notes 1. We routinely use Qiagen columns to prepare plasmid DNA, but other isolation procedures giving pure DNA should work as well. If problems are encountered, the lipopoly saccharide (LPS)-free plasmid purification kit could be used. The plasmid DNA is eluted with injectable water, and we make sure that the DNA concentration of the plasmid preparation is around 1 μg/μL or higher. This reduces the effect of the buffer the DNA is dissolved in on the pH of the transfection cocktail. 2. Although a high percentage of transfected 293T cells can be obtained with a variety of transfection protocols, we obtained the highest vector titers with the calcium phosphate coprecipitation method. The number of plasmid molecules delivered to each transfected cell might be particularly high with this method,


3.

4.

5. 6.

7.

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allowing high expression and ensuring cotransfection of each cell with all packaging and vectors constructs. The pH is critical for the formation of fine CaPO4-DNA precipitates. Therefore, for each new batch of 2× HBS buffer, we prepare 3 aliquots with pH values of 7.10, 7.12, and 7.14, respectively. Transfection efficiencies are compared, and the best aliquot is subsequently used. To avoid shifts in pH, freshly thawed 2× HBS and 2 M CaCl2 as well as injectable water are used to set up the transfection cocktail. The medium is changed 4–6 h prior to transfection to standardize the pH of the medium at the time of transfection. Medium, that was stored with a lot of air above the liquid, was occasionally observed to give poor results. It is also advisable to keep the number of cells plated constant. If transfection efficiency goes down, thawing fresh 293T cells often solves the problem. For titration, 293A cells, which are a subclone of 293 cells, are used since they adhere very well to the plates and form good monolayers. Titers on 293A cells are higher than on those on 293T cells. We previously concentrated vectors by ultracentrifugation as described (19). However, in our hands recovery rates were rather variable. If vector supernatants have to be concentrated more than 100-fold, ultracentrifugation should be used, since higher concentration by filtration leads to viscous solutions.

References 1. Poznansky, M., Lever, A., Bergeron, L., Haseltine, W., and Sodroski, J. (1991) Gene transfer into human lymphocytes by a defective human immunodeficiency virus type 1 vector. J. Virol. 65, 532–536. 2. Naldini, L., Blömer, U., Gallay, P., et al. (1996) In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 272, 263–267. 3. Reiser, J., Harmison, G., Kluepfel Stahl, S., etal. (1996) Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. Proc. Natl. Acad. Sci. USA 93, 15266–15271. 4. Poeschla, E. M., Wong-Staal, F., and Looney, D. J. (1998) Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors. Nat. Med. 4, 354–357. 5. Johnston, J. C., Gasmi, M., Lim, L. E., et al. (1999) Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. J. Virol. 73, 4991–5000. 6. Mitrophanous, K., Yoon, S., Rohll, J., et al. (1999) Stable gene transfer to the nervous system using a non-primate lentiviral vector. Gene Ther. 6, 1808–1818. 7. Schnell, T., Foley, P., Wirth, M., Münch, J., and Überla, K. (2000) Development of a self-inactivating, minimal lentivirus vector based on simian immunodeficiency virus. Hum. Gene Ther. 11, 439–447. 8. Mangeot, P. E., Negre, D., Dubois, B., et al. (2000) Development of minimal lentivirus vectors derived from simian immunodeficiency virus (SIVmac251) and their use for gene transfer into human dendritic cells. J. Virol. 74, 8307–8315.

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9. Khabbaz, R. F., Heneine, W., George, J.R., et al. (1994) Brief report: infection of a laboratory worker with simian immunodeficiency virus. N. Engl. J. Med. 330, 172–177. 10. Tang, H., Kuhen, K. L., and Wong-Staal, F. (1999) Lentivirus replication and regulation. Annu. Rev. Genet. 33, 133–370. 11. Emerman, M. and Malim, M. H. (1998) HIV-1 regulatory/accessory genes: keys to unraveling viral and host cell biology. Science 280, 1880–1884. 12. Yee, J. K., Miyanohara, A., LaPorte, P., et al. (1994) A general method for the generation of high-titer, pantropic retroviral vectors: highly efficient infection of primary hepatocytes. Proc. Natl. Acad. Sci.USA 91, 9564–9568. 13. Wagner, R., Graf, M. , Bieler, K., et al. (2000) Rev-independent expression of synthetic gag-pol genes of HIV-1 and SIV: implications for the safety of lentiviral vectors. Hum. Gene Ther. 11, 2403–2413. 14. Haas, J., Park, E. C., and Seed, B. (1996) Codon usage limitation in the expression of HIV-1 envelope glycoprotein. Curr. Biol. 6, 315–324. 15. Schneider, R., Campbell, M., Nasioulas, G., Felber, B. K., and Pavlakis, G. N. (1997) Inactivation of the human immunodeficiency virus type 1 inhibitory elements allows Rev-independent expression of Gag and Gag/protease and particle formation. J. Virol. 71, 4892–4903. 16. Cullen, B. R. (1986) Trans-activation of human immunodeficiency virus occurs via a bimodal mechanism. Cell 46, 973–982. 17. Malim, M. H., Hauber, J., Fenrick, R., and Cullen, B. R. (1988) Immunodeficiency virus rev trans-activator modulates the expression of the viral regulatory genes. Nature 335, 181–183. 18. DuBridge, R. B., Tang, P., Hsia, H. C., et al. (1987) Analysis of mutation in human cells by using an Epstein-Barr virus shuttle system. Mol. Cell Biol. 7, 379–387. 19. Yee, J. K., Friedmann, T., and Burns, J. C. (1994). Generation of high-titer pseudotyped retroviral vectors with very broad host range, in Methods in Cell Biology, vol. 43, Academic, New York, pp. 99–112. 20. Fouchier, R. A. M., Meyer, B. E., Simon, J. H. M., Fischer, U., and Malim, M. H. (1997) HIV-1 infection of non-dividing cells: evidence that the amino-terminal basic region of the viral matrix protein is important for Gag processing but not for post-entry nuclear import. EMBO J. 16, 4531–4539.

Cytoplasmic RNA Vector from Sendai Virus

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25 Cytoplasmic RNA Vector Derived from Nontransmissible Sendai Virus Production and Use Akihiro Iida and Mamoru Hasegawa 1. Introduction Sendai virus (SeV) is an enveloped virus with a nonsegmented negativestrand RNA genome of 15,384 nucleotides; it is a member of the Paramyxoviridae family (1–3). The virus is pneumotropic in rodent species such as mice and rats, but no pathogenicity has been reported in humans. SeV has been utilized for generation of hybrid cells between mammalian cells of different species in vitro by use of its cell fusion activity, and it has contributed to somatic cell genetics (4). The inactivated SeV has been also used for generation of a fusogenic viral liposome (hemagglutinating virus of Japan, or Sendai virus [HVJ]-liposome), which aimed to improve the efficiency of liposome-mediated DNA transfer (5,6). One of the characteristics of SeV is that replication occurs exclusively in the cytoplasm of infected cells and does not go through a DNA phase; thus there is no concern for unwanted integration of foreign sequences into chromosomal DNA. No need to transfer genetic materials to nuclei of target cells might be another advantage. Therefore, we expect that SeV may be a safer and more efficient viral vector than existing vectors for application to human therapy in various fields including gene therapy. Methods to rescue infectious SeV from cloned cDNA were established by two groups in 1995 and 1996, respectively (7,8). Since then, such reverse genetics technology allowed construction of genetically engineered SeVs, which carry additional foreign genes, and opened the way for the development of gene transfer vectors (Fig. 1). The addendum type of the vectors prepared by From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. Schematics of the SeV genome structures of wild type as well as recombinant addendum and F-defective types. The SeV genome is 15,384 nt long and its genes (NP, P, M, F, HN, and L) are in order from 3' to 5' in the nonsegmented negativestrand RNA. Addendum type has been constructed and reported previously (9–14). In the F-defective type, the entire F gene has been removed by PCR strategy, and transgenes can be introduced in a unique NotI site between the leader sequence and the NP gene. The text describes the introduction of the enhanced green fluorescent protein (EGFP) reporter gene between the M and HN genes.

this method have shown high efficiency of gene transfer and expression of foreign proteins in mammalian cells in vitro and in vivo (9–14). However, the recombinant SeVs constructed in these studies have contained all the viral structural genes and thus propagated virions that were fully infectious and capable of spreading in animal bodies. We have recently succeeded in establishing a method of constructing nontransmissible SeV vectors capable of self-replication in infected cells but incapable of infecting neighboring cells. This novel type of vector has been shown to keep the same ability of gene introduction and expression and is thus expected to be useful in human therapy (15). 1.1. Design of F-defective SeV Vectors The SeV genome has a leader and a trailer region at each of its 3' and 5' ends, and contains six major genes, which are lined up in tandem on single negativestrand RNA (Fig. 1). Initiation of replication and transcription of the viral genes occurs in the leader region in infected cells. SeV genomic RNA and the three virus proteins, the nucleoprotein (NP), phosphoprotein (P), and large protein (L; the catalytic subunit of RNA polymerase), form a ribonucleoprotein com-


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plex (RNP), which acts as a template for transcription and replication. Matrix protein (M) engages in the assembly and budding of viral particles. Two envelope glycoproteins, hemagglutinin-neuraminidase (HN) and fusion protein (F), mediate attachment of virions and penetration of RNPs into infected cells. HN protein binds to the cell surface sialic acids and then liberates them to make asialo receptors. F protein is essential for the infectivity of SeV; it is synthesized as an inactive precursor protein, F0, and then split into F1 and F2 by proteolytic cleavage of trypsin-like enzyme. In our intial design for nontransmissible SeV vectors, we deleted the F gene from the SeV genome of the attenuated Z strain (16) and replaced it with a reporter enhanced green fluorescence protein (EGFP) gene. EGFP expression was detectable in a single living cell, which allowed us to validate successful recovery of RNPs containing an Fdefective RNA genome inside such cells. For expressing additional foreign gene(s) of interest, the gene can be inserted in a unique NotI restriction enzyme cleavage site located between the start signal and the initiation ATG codon of the NP gene (9). The gene can be amplified by polymerase chain reaction (PCR) with transcriptional end (E) and restart (S) signals connected by a trinucleotide intergenic sequence at the 3' end and NotI recognition sequences at both ends (9). The length of the fragment should be a multiple of 6 bp, following rule of six for efficient SeV replication (17,18). 1.2. Construction of the Packaging Cell Line SeV F protein is required for the formation of infectious SeV particles. Therefore, recovery of SeV vectors from the RNA genome lacking the F gene has to be complemented with this gene in trans. We thus constructed an Fexpressing packaging LLC-MK2 cell line with a Cre/loxP-inducible expression system (19). LLC-MK 2 cells were transfected with the plasmid pCALNdLw/F (with the F gene located under the stuffer neo sequence, flanked by a pair of loxP sequences), and stable Neor clones were isolated. The recombinant adenovirus vector AxCANCre expressing Cre recombinase (20) was infected into these neor clones at a multiplicity of infection (MOI) of 3. Seven of 15 clones expressed F protein inducibly; the clone that showed the highest F protein was designated LLC-MK2/F7 and used as a packaging cell line for the F-defective SeV vectors. 1.3. Generation of F-defective SeV Vectors For generating F-defective SeV vectors, we have devised the following procedure, which consists of two steps (Fig. 2). The first step is to recover RNPs of F-defective RNA genome in LLC-MK2 cells using a plasmid bearing Fdefective cDNA and three other plasmids expressing NP, P, and L proteins,

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Fig. 2. System for generating the F-defective SeV vectors from SeV cDNAs carrying foreign genes. Step 1: LLC-MK2 cells are transfected with SeV cDNA defective in the F gene and the three plasmids encoding viral proteins, NP, P, and L, under the transcriptional control of T7 RNA polymerase. The enzyme is provided by the recombinant vaccinia virus vTF7-3 previously inactivated by psoralen and long-wave UV light (UV-vTF7-3). Transfection resulted in the formation of RNP complexes containing an F-defective RNA genome. Step 2: The reconstituted functional RNPs in step 1 are transfected into F-expressing LLC-MK 2/F7 cells with cationic liposome (DOSPER). RNP complexes are rescued to generate infectious viral particles (SeV vector), which are released into the supernatant of the cells.

respectively. All these cDNAs were under transcriptional control of the T7 promoter, which can be driven by T7 RNA polymerase from the recombinant vaccinia virus vTF7-3 (21). We confirmed the formation of functional RNPs by observing EGFP-expressing cells 3 days after transfection. Such cells were observed only when these four materials were cotransfected into LLC-MK2 cells. The second step is to transfect the RNPs into the F-expressing packaging cell line and to collect infectious particles (SeV vectors) from the supernatant. To raise the recovery efficiency of RNPs in the first step, we pretreated vTF73 with psoralen and long-wave UV irradiation. This treatment inactivated replication capability of the viruses without impairing infectivity and T7 RNA polymerase expression (22). We estimated the recovery frequency by the method as described previously (7) using wild-type SeV cDNA and inoculating the diluted lysates of transfected cells into embryonic hen eggs. With untreated vTF7-3, 1 infectious unit was detected from 105 transfected cells (7). However, with psoralen and long-wave UV-treated vTF7-3, 1 infectious unit


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was formed from 103 cells, indicating an improvement of nearly 100-fold. As to the F-defective SeV cDNA, the numbers of EGFP-expressing cells were scored to estimate the recovery efficiency of functional RNP. Under these conditions, such cells were detected approximately 1 in 105 transfected cells. The lysates containing functional RNPs were obtained by freeze and thaw cycles, mixed with cationic liposome, and transfected into F protein-expressing LLCMK2/F7 cells. The infectious virus particles were recovered in the culture supernatant, and the recovery efficiency was at least 1 infectious unit from 105 transfected cells. The particles were recovered only from LLC-MK2/F7 cells cultured with trypsin. When the cells were cultured in the absence of trypsin, scattered EGFP expression signals were detected, but they did not spread to neighboring cells. After passaging the supernatant to LLC-MK2/F7 cells, the infectious titer of the particles reached 0.5–1.0 × 108 cell infectious units (CIU)/mL. 1.4. Introduction and Expression of the EGFP Gene by F-Defective SeV Vectors in Cultured Cells SeV HN protein interacts with sialic acids, which exist in glycoproteins and glycolipids on the cell surface as the receptor, and thus permits the vectors to enter into a wide variety of cell types. Indeed, EGFP in the F-defective SeV vector can be expressed in various normal human cells including smooth muscle cells, hepatocytes, and lung microvascular endothelial cells, and in primary cultures of fetal rat hippocampal neurons. The infection are usually performed by incubating the cells for 1 h with an appropriate MOI of vector stock, after which the cells are incubated in complete medium. 2. Materials 2.1. Cell Culture 1. LLC-MK2 cell line (rhesus monkey kidney; ATCC CCL-7) and LLC-MK2/F7 cell line (see Subheading 1.2.): Cells were cultured at 37°C in a humidified 5% CO2 atmosphere. 2. MEM + 10% FCS: Eagle’s modified essential medium (MEM) supplemented with 10% heat-inactivated fetal calf serum (FCS), 100 U/mL penicillin, and 100 μg/mL streptomycin sulfate. 3. Cytosine arabinoside (Ara-C) stock solution: Dissolve Ara-C (Sigma) in H2O at 40 mg/mL, filter-sterilize, and store at –20°C. 4. 0.25% (w/v) trypsin solution. 5. MEM + Ara-C + trypsin: MEM supplemented with Ara-C at 40 μg/mL (1:1000 volume of Ara-C stock solution) and trypsin at 7.5 μg/mL (3:1000 volume of 0.25% trypsin solution). 6. MEM + trypsin: MEM supplemented with trypsin at 7.5 μg/mL.

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7. Phosphate-buffered saline (PBS): 170 mM NaCl, 3.4 mM KCl, 10 mM Na2HPO4, and 1.8 mM KH2PO4 (pH 7.2).

2.2. Psoralen and Long-Wave UV Light Inactivation of Recombinant Vaccinia Virus (UV-vTF7-3) 1. 2. 3. 4. 5.

Recombinant vaccinia virus stock (vTF7-3) (see Note 1). Bovine serum albumin fraction V solution (7.5% [w/v] BSA). 0.1% BSA/PBS: PBS containing 0.1% (w/v) BSA. STRATALINKER (Stratagene). Psoralen solution: Dissolve psolaren (Aldrich) in dimethyl sulfoxide (DMSO) at 1 mg/mL and store 1-mL aliquots at –20°C in the dark.

2.3. Inducible Expression of F Protein in LLC-MK2/F7 Cells 1. LLC-MK2/F7 cells in 6-well tissue culture dishes. 2. Recombinant adenovirus AxCANCre (RIKEN Gene Bank, RDB1748). 3. Anti-SeV F protein monoclonal antibody (f-236) (23) (see Note 2).

2.4. Generation of F-Defective SeV Vectors 1. Monolayers of LLC-MK2 cells in 100-mm tissue culture dishes. 2. Psoralen and long-wave UV-inactivated recombinant vaccinia virus vTF7-3 (UVvTF7-3). 3. SuperFect transfection reagent (Qiagen). 4. DNA materials: The plasmids pSeV18+b(+)/ΔF-EGFP (F-defective SeV cDNA with EGFP gene) (15) and pGEM-NP, pGEM-P, and pGEM-L, expressing NP, P, and L, respectively (24) (see Note 3). 5. Opti-MEM medium (Gibco-BRL). 6. Monolayers of F protein-induced LLC-MK2/F7 cells in 24-well tissue culture dishes. 7. DOSPER liposomal transfection reagent (Roche Diagnostic).

3. Methods 3.1. Generation of F-Defective SeV Vectors 3.1.1. Preparation of Psoralen and Long-Wave UV-Inactivated Recombinant Vaccinia Virus 1. Adjust the titer of vTF7-3 to 1 × 108 pfu/mL with 0.1% BSA/PBS. 2. Add psoralen solution to the virus suspension at 0.3 μg/mL and keep on ice for 10 min. 3. Transfer 1-mL aliquots of the virus suspension to 35-mm tissue culture dishes. 4. Irradiate 350-nm long-wave UV light to the virus suspension for 20 min using STRATALINKER. 5. Transfer 0.5-mL aliquots of the virus solution to 2-mL cryogenic vials and keep at –80°C until use.


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3.1.2. Inducible Expression of F Protein in LLC-MK2/F7 Cells 1. Day 1: Plate 5 × 105 LLC-MK2/F7 cells in 6-well tissue culture dishes and culture at 37°C overnight. 2. Day 2: Wash the cells once with MEM and infect the recombinant adenovirus AxCANCre at a MOI of 3. Tilt the dishes every 15 min to ensure uniform distribution of the virus adsorption and incubate at 37°C for 1 h. Wash the cells once with MEM, add 2 mL of MEM + 10% FCS, and incubate at 37°C for 2 days. 3. Day 4: Examine the expression of F protein by Western blotting using the anti-F protein monoclonal antibody f-236. The cells expressing F protein can be passaged within 20 generations in use for vector propagation.

3.1.3. Generation of F-Defective SeV Vectors from cDNA Stocks 1. Day 1: Plate 4 × 106 LLC-MK2 cells in 100-mm-diameter tissue culture dishes and incubate at 37°C overnight to 100% confluency. 2. Day 2: Wash the cells once with MEM and infect them with vTF7-3 at an MOI of 2. Tilt the dishes every 15 min at room temperature for 1 h to ensure uniform distribution of the virus adsorption. Wash the cells twice with MEM and transfect with a mixture containing pSeV18+b(+)/ΔF-EGFP (12 μg), pGEM-NP (4 μg), pGEM-P (2 μg), pGEM-L (4 μg), and 110 μL of SuperFect transfection reagent in 200 μL Opti-MEM, which was preincubated at room temperature for 10 min in a 15-mL polystyrene tube. Maintain the transfected cells in 3 mL of Opti-MEM with 3% FCS for 3 h, then wash them once with MEM and incubate in 10 mL MEM containing 40 μg/mL Ara-C for 60 h under 5% CO2 conditions. (See Notes 4 and 5). 3. Day 5: Examine EGFP expression of the transfected cells under fluorescence microscopy using a 450–490- and 500–550-nm exitation bandpass filter to validate the recovery of RNPs inside of the cells. Scrape the transfected cells from the dish, collect by centrifugation at 1000g for 5 min, resuspend in 800 μL OptiMEM, and lyse by three cycles of freezing and thawing. Mix the lysate with 600 μL of Opti-MEM and 200 μL of DOSPER in a 15-mL polystyrene tube for 15 min at room temperature. Transfect the F-expressing LLC-MK2/F7 cells in 24well tissue culture dishes with 200 μL each of the lysate mixture. 4. Day 6: 24 h after the transfection, wash the cells once with MEM and incubate in 0.5 mL MEM + Ara-C + trypsin for 3–6 days. 5. Days 9–12: Examine the spread of EGFP-expressing cells under fluorescence microscopy. Determine the vector titer by the method described in Subheading 3.3. The vector suspension can be passaged by addition of the supernatant to LLC-MK2/F7 cells and incubation for 2–5 days in MEM + Ara-C + trypsin. After centrifugation of the supernatant at 1000g for 5 min, aliquot the vector suspension and store at –80°C as the vector stock. Determine the final vector titer as indicated in Subheading 3.3. after quick thawing of the stock in a tube at 37°C for 5 min (see Notes 6 and 7).

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3.2. Propagation of F-Defective SeV Vectors 1. Day 1: Plate 5 × 106 cells of F protein-induced LLC-MK2/F7 cells in 100-mm tissue culture dishes and incubate overnight to approximately 100% confluency. 2. Day 2: Wash the cells once with MEM and infect with the SeV vector stock at an MOI of 0.1–1. Tilt the dishes every 15 min to distribute the inoculum and incubate at 37°C for 1 h. Wash the cells once with MEM and add 10 mL MEM + trypsin. Incubate the dishes at 37°C under 5% CO2 conditions. 3. Days 3–5: Harvest the supernatants every 24 h and replace with a fresh 10 mL of MEM + trypsin for 3 days. After centrifugation of the supernatant at 1000g for 5 min, aliquot the virus suspension, store at –80°C, and determine the vector titer.

3.3. Titration of F-Defective SeV Vectors by Cell Infectious Assay 1. Day 1: Plate 5 × 105 LLC-MK2 cells in 6-well tissue culture dishes. 2. Day 2: Prepare a series of tenfold dilutions of a vector stock in 1 mL MEM. Add the 100 μL of each dilution of the stock plus 900 μL MEM to the cells in duplicate. Tilt the dishes every 20 min and incubate at 37°C for 1 h. Wash the cells once with MEM and add 2 mL MEM + 10% FCS. 3. Day 4: Count the number of EGFP-expressing cells under a fluorescence microscope in triplicate. The total average number in the well can be obtained by multiplying this number by total area/counted area. The titer can be expressed as CIU/mL.

3.4. Infection of F-Defective SeV Vectors In Vitro 1. Infect cells with a vector stock at an appropriate MOI. Tilt the dishes every 15 min and incubate at 37°C for 1 h. Wash the cells once with MEM and add 10 mL complete medium. 2. Incubate for several days and examine the expression of EGFP under a fluorescence microscope and/or the gene(s) of interest by methods such as RT-PCR, Western blotting, or enzyme-linked immunosorbent assay.

4. Notes 1. The recombinant vaccinia virus vTF7-3 may be obtained from Dr. B. Moss (NIAID, NIH, Bethesda, MD). 2. Anti-F protein monoclonal antibody f-236 can recognize F0 protein but not F1 or F2 protein by Western blotting. The antibody can also be used for flow cytometric analysis of F-expressing cells. 3. All plasmid DNA samples should be prepared through cesium chloride gradients or commercial kits by ion-exchange chromatography. 4. The cytopathic effect by UV-vTF7-3 still exists and causes rounding and detaching of LLC-MK2 cells. Care must be taken when washing and changing the medium. 5. The ratio of NP-, P-, and L-expressing plasmids is an important determinant for the efficient recovery of RNP from SeV cDNA, as described in the ref. (7).


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6. The recombinant vaccinia virus vTF7-3 exists in SeV vector stock in early stages of passage even after the virus has been inactivated by psoralen and long-wave UV light. To remove the residual vaccinia virus, SeV vectors should be propagated in the medium containing Ara-C for several passages. The vaccinia virus can be detected by plaque assay (7). 7. Recovery of vectors is dependent on several factors such as cell density, transfection efficiency, and successful preparation of UV-vTF7-3. Improvements in the efficiency of the recovery procedure are in progress.

Acknowledgments We thank Atsushi Kato and Yoshiyuki Nagai at the National Institute of Infectious Disease in Tokyo, Japan, and Hai-Ou Li, Ya-Feng Zhu, Makoto Asakawa, Hidekazu Kuma, Takahiro Hirata, Yasuji Ueda, Yun-Sik Lee, and Masayuki Fukumura at DNAVEC Research Inc. for contributing to the work. References 1. Lamb, R. A. and Kolakofsky, D. (1996) Paramyxoviridae: the viruses and their replication,. In Virology, 3rd ed. (Fields, B. N., Knipe, D. M., and Howley, P. M., eds.), Lippincott-Raven, Philadelphia, pp. 1177-1204. 2. Conzelmann, K.-K. (1998) Nonsegmented nagative-strand RNA viruses: Genetics and manipulation of viral genomes. Ann. Rev. Genet. 32, 123–162. 3. Nagai, Y. and Kato, A. (1999) Paramyxovirus reverse genetics is coming of age. Microbiol. Immunol. 43, 613–624. 4. Okada, Y. and Tadokoro, J. (1962) Analysis of giant polynuclear cell formation caused by HVJ virus from Ehrlich’s ascites tumor cells. Exp. Cell. Res. 26, 98–128. 5. Kato, K., Nakanishi, M., Kaneda, Y., Uchida, T., and Okada, Y. (1991) Expression of hepatitis B virus surface antigen in adult rat liver. J. Biol. Chem. 26, 3361–3364. 6. Dzau, V., Mann, M., Morishita, R., and Kaneda, Y. (1996) Fusigenic viral liposome for gene therapy in cardiovascular diseases. Proc. Natl .Acad. Sci. USA 93, 11421–11425. 7. Kato, A., Sakai, Y., Shioda, T., et al. (1996) Initiation of Sendai virus multiplication from transfected cDNA or RNA with negative or positive sense. Genes Cells 1, 569–579. 8. Garcin, D., Pelet, T., Calain, P., et al. (1995) A highly recombinogenic system for the recovery of infectious Sendai paramyxovirus from cDNA. EMBO J. 14, 5773–5784. 9. Hasan, M. K., Kato, A., Shioda, T., et al. (1997) Creation of an infectious recombinant Sendai virus expressing the firefly luciferase from 3' proximal first locus. J. Gen. Virol. 78, 2813–2820. 10. Moriya, C., Shioda, T., Tashiro, K., et al. (1998) Large quantity production with extreme convenience of human SDF-1α and SDF-1β by a Sendai virus vector. FEBS Lett. 425, 105–111.

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11. Yu, D., Shioda, T., Kato A., et al. (1997) Sendai virus-based expression of HIV-1 gp120: reinforcement by the V(-) version. Genes Cells 2, 457–466. 12. Sakai, Y., Kiyotani, K., Fukumura, M., et al. (1999) Accommodation of foreign genes into the Sendai virus genome: sizes of inserted genes and viral replication. FEBS Lett. 456, 221–226. 13. Toriyoshi, H., Shioda, T., Sato, H., et al. (1999) Sendai virus-based production of HIV type 1 subtype B and subtype E envelope glycoprotein 120 antigen and their use for highly sensitive detection of subtype-specific serum antibody. AIDS Res. and Hum. Retroviruses 12, 1109–1120. 14. Yonemitsu Y., Kitson, C., Ferrari, S., et al. (2000) Efficient gene transfer to airway epithelium using recombinant Sendai virus. Nat. Biotechnol. 18, 970–973. 15. Li, H-O., Zhu, Y-H., Asakawa, M., et al. (2000) A cytoplasmic RNA vector derived from nontransmissible Sendai virus with efficient gene transfer and expression. J. Virol. 74, 6564–6569. 16. Shioda, T., Iwasaki, K., and Shibuta, H. (1986) Determination of the complete nucleotide sequence of Sendai virus genome RNA and the predicted amino acid sequence of the F, HN, and L proteins. Nucleic Acids Res. 14, 1545–1563. 17. Calain, P. and Roux, L. (1993) The rule of six, a basic feature for efficient replication of Sendai virus defective interfering RNA. J. Virol. 67, 4822–4830. 18. Korakofsky, D., Pelet, T., Garcin, D., et al. (1998) Paramyovirus RNA synthesis and requirement for hexamer genome length: the rule of six revisited. J. Virol. 72, 891–899. 19. Arai, T., Matsumoto, K., Saitoh, K., et al. (1998) A new system for stringent, high-titer vesicular stomatitis virus G protein-pseudotyped retrovirus vector induction by introduction of Cre recombinase into stable prepackaging cell lines. J. Virol. 72, 1115–1121. 20. Kanegae, Y., Takamori K., Sato, Y., et al. (1996) Efficient gene activation system on mammalian cell chromosome using recombinant adenovirus producing Cre recombinase. Gene 181, 207–212. 21. Fuerst, T. R., Niles, E. G., Studier, F. W., and Moss, B. (1986) Eukaryotic transient-expression system based on recombinant vaccinia virus that synthesizes bacteriophage T7 RNA polymerase. Proc. Natl. Acad. Sci. USA 83, 8122–8126. 22. Tsung, K., Yim, J. H., Marti, W., Buller, R. M. L., and Norton, J. A. (1996) Gene expression and cytopathic effect of vaccinia virus inactived by psoralen and longwave UV light. J Virol. 70, 165–171. 23. Segawa, H., Kato, M., Yamashita, T., and Taira, H. (1998) The role of individual cysteine residues of Sendai virus fusion protein in intracellular transport. J. Biochem. 123, 1064–1072. 24. Curran, J., Boeck, R., and Kolakofsky, D. (1991) The Sendai virus P gene expresses both an essential protein and an inhibitor of RNA synthesis by shuffling modules via mRNA editing. EMBO J. 10, 3079–3085.

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26 Preparation of Helper-Dependent Adenoviral Vectors Philip Ng, Robin J. Parks, and Frank L. Graham 1. Introduction 1.1. First-Generation Adenovirus Vector Adenoviruses (Ads) are excellent mammalian gene transfer vectors because of their ability to infect efficiently a wide variety of quiescent and proliferating cell types from various species to direct high-level gene expression. Consequently, Ad vectors are extensively used as potential recombinant viral vaccines, for high-level protein production in cultured cells and for gene therapy (1–4). First-generation Ad vectors typically have foreign DNA inserted in place of early region 1 (E1). E1-deleted vectors are replication deficient and are propagated in E1-complementing cells such as 293 (5). Although these vectors remain very useful for many applications, it has become clear that transgene expression in vivo is only transient. Several factors contribute to this, including strong innate and inflammatory responses to the vector (6,7), acute and chronic toxicity caused by low-level viral gene expression from the vector backbone (8), and generation of anti-Ad cytotoxic T-lymphocytes caused by de novo viral gene expression (9–12) or processing of virion proteins (13). Although high-level transient transgene expression afforded by first-generation Ad vectors may be adequate, or even desirable, for many gene transfer and gene therapy applications, the transient nature of expression kinetics renders these vectors unsuitable when prolonged, stable expression is required. 1.2. Helper-Dependent Adenovirus Vector In principle, the simplest way to eliminate Ad-induced toxicity caused by expression of viral proteins is to remove all viral coding sequences from the From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. The Cre/loxP system for generating HD vectors. 293Cre cells are coinfected with the HD vector and a helper virus bearing a packaging signal flanked by loxP sites. Cre-mediated excision of the packaging signal (ψ) renders the helper virus genome unpackageable but does not interfere with its ability to provide all the necessary transacting factors for propagation of the HD vector. The titer of the HD vector is increased by serial passage in helper virus-infected 293Cre cells. The HD vector need contain only those Ad cis-acting elements required for DNA replication (ITRs) and encapsidation (ψ); the remainder of the genome consists of the desired transgene and non-Ad stuffer sequences.

vector. In the absence of cell lines that contain and express the entire Ad genome, a “helper” Ad is required to provide all necessary functions in trans for propagation of these fully deleted, helper-dependent (HD) vectors. The only Ad sequences required in cis for viral replication are the inverted terminal repeats (ITRs) necessary for DNA replication and the packaging signal (ψ) necessary for encapsidation of the vector genome. These cis-acting elements amount to only 500 bp. HD vectors retain all the benefits of first-generation Ad vectors but have the added advantage of increased cloning capacity (37 kb), and it is now becoming clear that they offer the potential for reduced toxicity and prolonged, stable transgene expression (14–21). The purpose of this chapter is to provide a detailed protocol for the preparation of HD vectors. The reader is referred elsewhere for excellent, comprehensive reviews on HD vectors (22,23).


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1.3. Overview of the Helper-Dependent Adenovirus Vector System A critical feature of this system is a method of inhibiting helper virus propagation without interfering with its ability to provide helper functions for propagation of the HD vector. To date, the most efficient means of achieving this goal is the Cre/loxP method developed by Graham and co-workers (Fig. 1) (24). In this system the packaging signal of the helper virus is flanked by loxP sites. Thus, following infection of 293 cells expressing Cre recombinase, such as 293Cre4 cells (25), the packaging signal is excised from the helper virus by Cre-mediated site-specific recombination between the loxP sites, rendering the genome unpackageable. However, the ability of the viral DNA to replicate and provide helper functions in trans for propagation of a coinfected HD vector is not impaired. The titer of the HD vector is increased by serial coinfection of 293Cre cells with the HD vector and the helper virus. In the last step, the HD vector is purified by CsCl ultracentrifugation. Although a number of factors can influence the yield and purity of HD vectors (see Subheading 3.), typically about 10 10–10 11 virus particles are produced per 150-mm dish of coinfected cells with a helper virus contamination level of ≤0.1% using the method described in Subheading 3. 2. Materials 2.1. Cell Culture 1. Low-passage 293 and 293Cre4 cells. 2. Complete medium: Minimum essential medium (MEM; Gibco-BRL cat. no. 61100) containing 10% fetal bovine serum (FBS) (heat inactivated), 100 U/mL penicillin/streptomycin, 2 mM L-glutamine, and 2.5 μg/mL fungizone. 3. G418. 4. Citric saline: 135 mM KCl, 15 mM sodium citrate, autoclave-sterilized

2.2. Helper-Dependent Adenovirus Vector The helper-dependent vector contains the expression cassette of interest and 500 bp of cis-acting Ad sequences necessary for vector DNA replication (ITRs) and packaging (ψ). In addition to these minimal Ad sequences, Sandig et al. (26) have shown that inclusion of a small segment of noncoding Ad sequence from the E4 region adjacent to the right ITR increases vector yields, possibly by enhancing packaging of the vector DNA. The size of the vector is an important consideration. For efficient packaging the Ad DNA should be between 75% (>27 kb) (27) and 105% (90% of the cells rounded up and detached from the dish) should be observed by about 48 h postinfection, at which time the cells are scraped into the medium. Then transfer 1 mL of the cell suspension to a microfuge tube for extraction of total DNA to monitor vector amplification (see Subheading 3.3.1.) and transfer the remainder into a 15-mL polypropylene tube and store at –70°C after adding 0.1 vol 40% sucrose. Thaw the lysate at 37°C and use 0.4 mL to coinfect a 60-mm dish of 90% confluent 293Cre4 cells with helper virus at an MOI of 1 pfu/cell. Adsorb for 1 h in the incubator, occasionally rocking the dishes. Add 5 mL of maintenance medium to the monolayer 1 h postinfection. Optional: For the LacZ control vector, infect a 60-mm dish of 90% confluent 293 cells with an appropriate volume (start with 0.4 mL of the transfection/infection lysate and reduce volume accordingly as the titer increases with serial passage) of the lysate (no helper virus is added) as described above. Twenty-four hours later, remove the medium and fix the monolayer by adding 1 mL of β-gal fix solution and incubating the dish at 37°C for 5 min. Remove the β-gal fix solution and add 2 mL of β-gal stain solution supplemented with 0.5 mg/mL X-gal. Incubate the dishes at room temperature in the dark and determine the vector titer the next day by counting blue cells. For serial passages of the vector, complete CPE should be observed by about 48 h postcoinfection (see Note 4), at which time the cells are scraped into the medium. Transfer 1 mL of the cell suspension to a microfuge tube for extraction of total DNA (see Subheading 3.3.1.), and transfer the remainder to a 15-mL polypropylene tube and store it at –70°C after adding 0.1 vol 40% sucrose. Repeat steps 9 and 10 to increase the titer of the HD vector. Typically, the vector

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Fig. 4. Amplification of the HD vector AdC4HSULacZ by serial passage using AdLC8cluc-infected 293Cre4 cells. The titer (blue-forming units [bfu]/mL) of the HD vector was determined at each passage, as described in Subheading 3.2.

titer increases 10- to 100-fold per passage, and six to eight serial passages are performed (Fig. 4) (see Note 5).

3.3. Monitoring Helper-Dependent Vector Amplification Once six to eight serial passages have been performed, a passage is chosen for large-scale preparation of the vector. Ideally, this passage should contain the maximum amount of HD vector and the minimum amount of helper virus. To determine which passage best meets these criteria, the amounts of vector DNA and helper DNA are determined by Southern blot analysis of the DNA extracted from each passage (see Note 6 for an alternative procedure to expedite vector production). 3.3.1. Extraction of Total DNA 1. Spin lysate collected as in Subheading 3.2., steps 8 and 10, in a microcentrifuge for 5 min at 750g to pellet infected cells. 2. Discard the supernatant and add 200 μL of pronase-SDS solution (see Subheading 2.4.) to pellet. 3. Resuspend the cell pellet and incubate overnight at 37°C. 4. Add 200 μL dH20 and precipitate DNA by adding 1 mL 95% ethanol. Mix by inverting the tube until a visible precipitate is formed. 5. Pellet the DNA by spinning in a microcentrifuge for 2 min at maximum speed. 6. Wash the DNA twice with 70% ethanol and dry.


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7. Resuspend the DNA in an appropriate volume (usually 30–35 μL) of TE (see Note 7).

We use Southern blot hybridization analysis with a packaging signal probe to determine the relative amount of potentially packageable HD vector and helper virus genomes in each passage (Fig. 5) (see Note 8). PCR-based methods may also be used for this purpose (26). Large-scale preparation of the HD vector is performed on the passage with the highest HD vector to helper virus ratio (see Subheading 3.4.). If several passages meet this criterion, then the earliest passage should be chosen since the chance of rearrangement of either the vector or helper may increase with higher passage numbers. 3.4. Large Scale Preparation and Purification of Helper-Dependent Vector Once the optimal passage has been determined as described in Subheading 3.3., large-scale preparation of the HD vector can be performed. This is accomplished by coinfecting 150-mm dishes of 90% confluent 293Cre4 cells (seeded 1–2 days previously in nonselective complete medium) with 1 mL of lysate from the passage previous (relative to the optimum passage) and helper virus at an MOI of 1 pfu/cell. (High-titer stock is typically used to minimize the volume.) Cells are coinfected for 1 h in the incubator and the dishes are rocked every 10–15 min, following which 15 mL of maintenance medium is added to each dish. The amount of HD vector desired dictates the number of dishes coinfected. As more dishes are required, more lysate from the previous passage will be required. This necessitates repeating and scaling up the appropriate earlier passages to generate enough inoculum (see Note 9). Complete CPE should be observed 48 h postinfection, at which time the cells are scraped into the medium and the cell suspension is harvested for extraction and purification of the HD vector. The protocol given below is for processing up to 20 150-mm dishes and should be scaled up accordingly for more dishes. 1. Harvest cells and medium into a suitable centrifuge bottle and centrifuge at 750g for 10 min. 2. Discard supernatant and resuspend cell pellet with 10 mL of 100 mM Tris-HCl, pH 8.0, and transfer into a 50-mL conical tube. Samples can be stored at –70°C. 3. Thaw samples if necessary and add 1 mL 5% sodium deoxycholate to lyse cells. Incubate at room temperature for 30 min with occasional mixing. The lysate should become highly viscous. 4. Add 100 μL 2 M MgCl2 and 50 μL DNAase I to digest the cellular and unpackaged viral DNA. Incubate at 37°C for 1 h mixing every 10 min. The viscosity should be greatly reduced.

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Fig. 5. Analysis of amplification of AdC4HSULacZ by serial passage using AdLC8cluc-infected 293Cre4 cells. (A) BglI restriction map of AdC4HSULacZ and AdLC8cluc. Probe ψ is composed of two synthetic oligonucleotides: 5' CCG GTG TAC ACA GGA AGT GAC AAT TTT CGC GCG GTT TTA GGC GGA TGT TGT AGT AAA TTT GGG CGT AAC CGA GTA AGA TTT GGC CAT TTT CGC GGG AAA ACT GAA TAA GAG GAA GTG AAA TCT GAA TAA TTT TGT GTT ACT CAT AGC GCG TAA T 3' and


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5. Spin the lysate at maximum speed for 15 min at 5°C in a Beckman tabletop centrifuge. 6. Meanwhile, prepare CsCl step gradient (1 Beckman SW41 Ti ultraclear tube for each 5 mL of lysate): Add 0.5 mL of 1.5 g/mL solution to tube. Gently overlay with 3 mL of 1.35 g/mL solution. Gently overlay 3 mL of 1.25 g/mL solution. 7. Apply 5 mL of supernatant from step 5 to the top of the gradient. If necessary, top up the tubes with 100 mM Tris-HCl, pH 8.0. 8. Spin at 35,000 rpm in a Beckman SW41 Ti rotor (151,000g) for 1 h at 10°C. 9. Collect virus band (should be at 1.25/1.35 interface) with a needle and syringe by piercing the side of the tube. The volume collected is unimportant at this stage, so try to recover as much of the virus band as possible. Pool virus bands, if more than one tube was used, into a Beckman SW 50.1 ultraclear tube. 10. Fill the tube with 1.35 g/mL solution and centrifuge in a Beckman SW 50.1 rotor at 35,000 rpm (151,000g) for 16–24 h at 4°C. 11. To collect the virus band, puncture the side of the tube just below the virus band with a needle and syringe. Collect the virus band in the smallest volume possible and transfer to a Slide-A-Lyzer dialysis cassette. Dialyze at 4oC against three changes of 500 mL 10 mM Tris-HCl, pH 8.0, for at least 24 h total. 12. Transfer the virus into a suitable vial and add sterile glycerol to a final concentration of 10%. Store at –70°C.

Typically, only one virus band is visible after step 11. However, on occasion, more than one band may be observed. In this case, the HD vector is expected to be the higher band (lower buoyant density), and the helper virus is expected to be the lower band (higher buoyant density) because of differences 5' A TTA CGC GCT ATG AGT AAC ACA AAA TTA TTC AGA TTT CAC TTC CTC TTA TTC AGT TTT CCC GCG AAA ATG GCC AAA TCT TAC TCG GTT ACG CCC AAA TTT ACT ACA ACA TCC GCC TAA AAC CGC GCG AAA ATT GTC ACT TCC TGT GTA CAC CGG 3'. These are 100% homologous to the packaging signals of AdC4HSULacZ and AdLC8cluc. (B) Approximately equivalent amounts of total DNA (as determined by OD260) extracted from each passage were digested with BglI, and the DNA fragments were separated by electrophoresis through a 1% agarose gel. 293 + AdLC8cluc represents total DNA extracted from AdLC8cluc-infected 293 cells, and 293Cre4 + AdLC8cluc represents total DNA extracted from AdLC8cluc-infected 293Cre4 cells. Serial passage number 0 refers to the initial transfection/infection. pC4HSULacZ was digested with PmeI and BglI. M, 1 kb PLUS DNA Marker (Gibco-BRL). (C) DNA from the agarose gel depicted in (B) was transferred to a nylon membrane and subjected to Southern blot hybridization analysis using the [α-32P]dCTP random primelabeled probe ψ. The band visible between 0.85 and 0.65 kb is not packaged and may represent the excised circular DNA bearing the packaging signal from AdLC8cluc (P. Ng and F. Graham, unpublished results).

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in their genome size (see Subheading 2.2.). All bands should be collected for analysis (see Note 10). If necessary, step 10 may be repeated to achieve higher purity. 3.5. Helper-Dependent Vector Characterization Following purification of the HD vector, several basic characterizations should be performed: 1) the concentration of virus particles should be determined; 2) the DNA structure should be analyzed to confirm that the vector has not rearranged; and 3) the level of helper virus contamination should be ascertained. The concentration of vector particles in the purified preparation is determined spectrophotometrically as follows: 1. Dilute (usually 20-fold) purified virus with TE supplemented with SDS to 0.1%. Set up blank the same except add virus storage buffer (10 mM Tris-HCl, pH 8.0, supplemented with glycerol to 10%) instead of virus. 2. Incubate for 10 min at 56°C. 3. Vortex sample briefly. 4. Determine OD260. 5. Calculate the number of particles/mL based on the extinction coefficient of wildtype Ad as determined by Maizel et al. (31) and corrected for the size difference between wild-type Ad and the HD vector as follows: (OD260)(dilution factor)(1.1 × 1012)(36)/(size of vector in kb)

Virion DNA is extracted and analyzed to confirm the proper structure and the level of helper virus contamination as follows: 1. Add an appropriate volume (25–100 μL depending on the vector concentration) of the purified virus to 0.4 mL of pronase-SDS solution and incubate overnight at 37°C to lyse the virions and digest virion proteins. 2. Precipitate virion DNA by adding 1/10 vol 3 M NaAcetate, pH 5.2, and 2.5 vol 95% ethanol and incubate at –20°C for 15–30 min. 3. Spin in a microcentrifuge for 10–15 min at maximum speed. 4. Discard the supernatant and wash the DNA pellet twice with 70% ethanol. 5. Dry the DNA pellet and resuspend in an appropriate volume of TE.

A sample of the vector DNA is digested with the appropriate diagnostic restriction enzyme(s) and the structure of the DNA is confirmed by ethidium bromide staining following agarose gel electrophoresis (see Note 11). To determine the level of helper virus contamination, the DNA can be transferred to a suitable membrane for Southern blot analysis with the packaging signal probe, and the relative intensities of the HD vector and helper virus-derived bands can


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be compared by phosphoimager analysis. Alternatively, PCR-based methods can be used (26). The amount of helper virus can also be ascertained by determining the number of pfu/mL following titration on 293 cells. However, a comparable unit of measurement for the HD vector cannot be obtained by this method. In addition to these standard characterizations, the biologic activity of the HD vector, with respect to expression of the transgene of interest, should also be determined. This will be unique to the vector in question, and appropriate assays should be employed in each case. 4. Notes 1. It is essential that the helper virus titer be accurately known. Thus, duplicate, independent titrations should be performed on both the high-titer and diluted working stocks. 2. High transfection efficiency is important for achieving a high initial concentration of vector for subsequent amplification. We use the calcium-phosphate coprecipitation method (32), but other methods may also be suitable. 3. The reporter vector and the vector of interest should be as similar as possible (i.e., same backbone, site, and orientation of transgene insertion, similar size, and so on). 4. If complete CPE is not observed by 48 h post infection, then the titer of the helper virus is probably lower than expected. If complete CPE was observed for previous passages, then discard the current working stock of diluted helper virus and repeat the passage using a different aliquot. Otherwise retitrate the helper virus and start the amplification over. 5. The titer of a LacZ vector typically reaches a peak of 108–109 blue-forming units (bfu)/mL. With subsequent passages, the titer may fluctuate (cf. Fig. 4) but should not drop and remain below 107 bfu/mL. 6. We have observed that the amplification kinetics of a LacZ control vector closely parallel that of many HD vectors when the conditions in Note 3 have been met (unpublished results). Therefore, to expedite vector production, large-scale vector preparation (see Subheading 3.4.) may be performed on the passage number of the HD vector that is equivalent to the passage number of the LacZ control vector when peak titer is first reached. 7. DNA prepared by this method does not dissolve easily. Heat the DNA at 65°C with occasional vortexing at maximum setting until dissolved. 8. Do not misinterpret results from eithium bromide-stained gels (Fig. 5B); the presence of helper virus-specific DNA fragments does not necessarily imply the presence of infectious helper virions since viral DNA from which the packaging signal has been excised can still replicate. For example, in Figure 5B, comparable amounts of helper virus DNA are observed in the control lanes (293 + AdLC8cluc and 293Cre4 + AdLC8cluc). However, Southern analysis with a packaging signal probe, which hybridizes equally to the packaging signals of both the HD vector

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and the helper virus, reveals that the amount of potentially packageable helper virus genomes is drastically lower (Fig. 5C). Furthermore, if total DNA is analyzed, as in Figure 5, this method cannot accurately determine the level of helper contamination since all DNA molecules containing the packaging signal will hybridize to the probe but may or may not be packaged. Also, any differences in packaging efficiencies will render such comparisons invalid. In contrast, if DNA extracted from virions is used for this analysis (e.g., from CsCl-purified virus; see Subheading 3.4.), then direct comparison between the intensity of the HD vector and helper virus-derived bands should be an accurate measure of the level of helper virus contamination. Although an effort should be made to load the same amount of DNA in each lane, there nevertheless may be variability, thus rendering comparisons between lanes not strictly valid. 9. The amplification kinetics for a given HD vector are fairly predictable. Therefore, once this has been established, scale-up can begin at the appropriate passage for future amplifications of that HD vector to avoid repeating and scaling up previous passages. 10. The higher virus band is collected first and, without removing the syringe from the tube, the lower band collected next with a second syringe. Care must be taken to collect the vector from the gradient with minimal contamination from the helper, even if only one band is visible. 11. If the amount of extracted virion DNA is low, then the DNA fragments may be undetectable by eithium bromide staining. In this case, the DNA can be transferred onto a suitable membrane for Southern blot analysis using the HD vector plasmid DNA as the probe.

Acknowledgments This work was supported by grants from the National Institutes of Health, the Medical Research Council of Canada (MRC), the National Cancer Institute of Canada (NCIC), and by Merck Research Laboratories. P. N. is supported by an MRC Postdoctoral Fellowship. References 1. Berkner, K. L. (1988) Development of adenovirus vectors for expression of heterologous genes. Biotechniques 6, 616–629. 2. Graham, F. L. and Prevec, L. (1992) Adenovirus-based expression vectors and recombinant vaccines, in Vaccines: New Approaches to Immunological Problems (Ellis, R. W., ed.), Butterworth-Heinemann, Boston, pp. 363–389. 3. Hitt, M., Addison, C. L., and Graham, F. L. (1997) Human adenovirus vectors for gene transfer into mammalian cells. Adv. Pharmacol. 40, 137–206. 4. Hitt, M. M., Parks, R. J., and Graham, F. L. (1999) Structure and genetic organization of adenovirus vectors, in The Development of Human Gene Therapy (Friedman, T., ed.), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, pp. 61–86.


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5. Graham, F. L., Smiley, J., Russell, W. C., and Nairn, R. (1977) Characteristics of a human cell line transformed by DNA from human adenovirus 5. J. Gen. Virol. 36, 59–72. 6. Wolf, G., Worgall, S., Van, R. N., Song, W. R., Harvey, B. G., and Crystal, R. G. (1997) Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ. J. Virol. 71, 624–629. 7. Worgall, S., Wolff, G., Falck-Pedersen, E., and Crystal, R. G. (1997) Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration. Hum. Gene Ther. 8, 37–44. 8. Morral, N., O’Neal, W., Zhou, H., Langston, C., and Beaudet, A. (1997) Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: comparison of E2a wildtype and E2a deleted vectors. Hum. Gene Ther. 8, 1275–1286. 9. Dai, Y., Schwartz, E. M., Gu, D., et al. (1995) Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression. Proc. Natl. Acad. Sci. USA 92, 1401–1405. 10. Yang, Y., Nunes, F. A., Berencsi, K., et al. (1994) Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc. Natl. Acad. Sci. USA 91, 4407–4411. 11. Yang, Y., Li, Q., Ertl, H. C., and Wilson, J. M. (1995) Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses. J. Virol. 69, 2004–2015. 12. Yang, Y., Xiang, Z., Ertl, H. C., and Wilson, J. M. (1995) Upregulation of class I major histocompatibility complex antigens by interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivo. Proc. Natl. Acad. Sci. USA 92, 7257–7261. 13. Kafri, T., Morgan, D., Krahl, T., et al. (1998) Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: implications for gene therapy. Proc. Natl. Acad. Sci. USA 95, 11377–11382. 14. Chen, H-H., Mack, L. M., Kelly, R., et al. (1997) Persistence in muscle of an adenoviral vector that lacks all viral genes. Proc. Natl. Acad. Sci. USA 94, 1645–1650. 15. Morral., N., Parks, R. J., Zhou, H., et al. (1998) High doses of a helper-dependent adenoviral vector yield supraphysiological levels of α1-antitrypsin with negligible toxicity. Hum. Gene Ther. 9, 2709–2716. 16. Morsy, M. A., Gu, M., Motzel, S., et al. (1998) An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc. Natl. Acad. Sci. USA 95, 7866–7871. 17. Schiedner, G., Morral, N., Parks, R. J., et al. (1998) Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity. Nat. Genet. 18, 180–183. 18. Morral, N., O’Neal, W., Rice, K., et al. (1999) Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for

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long-term liver directed gene transfer in baboons. Proc. Natl. Acad. Sci. USA 96, 12816–12821. Balague, C., Zhou, J., Dai, Y. et al. (2000) Sustained high-level expression of full-length human factor VIII and restoration of clotting activity in hemophilic mice using a minimal adenovirus vector. Blood 95, 820–828. Cregan, S. P., MacLaurin, J., Gendron, T. F., et al. (2000) Helper-dependent adenovirus vectors: their use as a gene delivery system to neurons. Gene Ther. 14, 1200–1209. Maione, D., Wiznerowicz, M., Delmastro, P., et al. (2000) Prolonged expression and effective readministration of erythropoietin delivered with a fully deleted adenoviral vector. Hum. Gene Ther. 11, 859–868. Kochanek, S. (1999) High-capacity adenoviral vectors for gene transfer and somatic gene therapy. Hum. Gene Ther. 10, 2451–2459. Parks R. J. (2000) Improvements in adenoviral vector technology: overcoming barriers for gene therapy. Clin. Genet. 58, 1–11. Parks, R. J., Chen, L., et al. (1996) A helper-dependent adenovirus vector system: removal of helper virus by Cre-mediated excision of the viral packaging signal. Proc. Natl. Acad. Sci. USA 93, 13565–13570. Chen, L., Anton, M., and Graham, F. L. (1996) Production and characterization of human 293 cell lines expressing the site-specific recombinase Cre. Somat. Cell Mol. Genet. 22, 477–488. Sandig, V., Youil, R., Bett, A. J., et al. (1999) Optimization of the helper-dependent adenovirus system for production and potency in vivo. Proc. Natl. Acad. Sci. USA 97, 1002–1007. Parks, R. J. and Graham, F. L. (1997) A helper-dependent system for adenovirus vector production helps define a lower limit for efficient DNA packaging. J. Virol. 71, 3293–3298. Bett, A. J., Prevec, L., and Graham, F. L. (1993) Packaging capacity and stability of human adenovirus type 5 vectors. J. Virol. 67, 5911–5921. Parks, R. J., Bramson, J. L., Wan, Y., Addison, C. L., and Graham, F. L. (1999) Effects of stuffer DNA on transgene expression from helper-dependent adenovirus vectors. J. Virol. 73, 8027–8034. Parks, R. J., Evelegh, C. M., and Graham, F. L. (1999) Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration. Gene Ther. 6, 1565–1573. Maizel, J. V., White, D., and Scharff. M. D. (1968) The polypeptides of adenovirus. I. Evidence of multiple protein components in the virion and a comparison of types 2, 7a, and 12. Virology 36, 115–125. Graham, F. L. and van der Eb, A. J. (1973) A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology 52, 456–467.

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27 Construction of First-Generation Adenoviral Vectors Philip Ng and Frank L. Graham

1. Introduction Adenoviruses (Ads) possess several features that make them attractive as mammalian gene transfer vectors. They can efficiently infect a wide variety of quiescent and proliferating cell types from various species to direct high-level viral gene expression, their 36-kb double-stranded DNA genome can be manipulated with relative ease by conventional molecular biology techniques, and they can be readily propagated and purified to yield high-titer preparations of very stable virus. Consequently, Ads have been extensively used as vectors for recombinant vaccines, for high-level protein production in cultured cells and for gene therapy (1–4). 1.1. Adenovirus Biology The adenovirus is an icosohedral, nonenveloped capsid containing a linear double-stranded DNA genome of approx 36 kb. Of the approximately 50 serotypes of human Ad, serotype 2 (Ad2) and serotype 5 (Ad5) of subgroup C have been the most extensively characterized (reviewed in ref. 5). The 36-kb genome is flanked by inverted terminal repeats (ITRs), which are the only sequences required in cis for DNA replication. A cis-acting packaging signal, required for encapsidation of the genome, is located near the ITR at the left end (relative to the conventional map of Ad). The Ad genome can be divided into two regions with respect to the onset of viral DNA replication (Fig. 1).The early region genes, E1A, E1B, E2, E3, and E4, are expressed before DNA replication. The


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Fig. 1. Transcription map of human adenovirus serotype 5. The 100 map unit (approx 36 kb) genome is divided into four early region transcription units, E1–E4, and five families of late mRNA, L1–L5, which are alternative splice products of a common late transcript expressed from the major late promoter (MPL) located at 16 mu. Four smaller transcripts are also produced, pIX, IVa, and VA RNAs I and II. Not shown are the 103-bp inverted terminal repeats located at the termini of the genome involved in viral DNA replication and the packaging signal located from nucleotides 190 to 380 at the left end of the genome involved in encapsidation.

E1A transcription unit is the first Ad sequence expressed during viral infection and encodes two major E1A proteins that are involved in transcriptional regulation of the virus and stimulation of the host cell to enter S phase. The two major E1B proteins are necessary for blocking host mRNA transport, stimulating viral mRNA transport, and blocking E1A-induced apoptosis. The E2 region encodes proteins required for viral DNA replication and can be divided into to subregions, E2a and E2b. E2a encodes the 72-kDa DNA-binding protein, and E2b encodes the viral DNA polymerase and terminal protein precursor. The E3 regions encodes at least seven proteins, most of which are involved in evasion of the host immune system. This region is dispensable for virus growth in cell culture. The E4 region encodes at least six proteins, some of which function in facilitating DNA replication, enhancing late gene expression, and decreasing host protein systhesis. The late region genes, L1–L5, are expressed after DNA replication from a common major late promoter and are generated from alter-


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native splicing of a single transcript. Most of the late mRNAs encode virion structural proteins. Virus infection begins with the Ad fiber protein binding to specific primary receptors on the cell surface (6,7) followed by a secondary interaction between the virion penton base and αvβ3 and αvβ5 integrins (8). The efficiency with which Ad binds and enters the cell is directly related to the level of primary and secondary receptors present on the cell surface (9,10). Penton-integrin interaction triggers Ad internalization by endocytosis; it then escapes from the early endosome into the cytosol prior to lysosome formation (11,12). The virion is sequentially disassembled during translocation along the microtubule network toward the nucleus, where the viral DNA is released into the nucleus (13). Viral DNA replication, beginning 6–8 h post infection, and assembly of progeny virions occur in the nucleus. The entire life cycle takes about 24–36 h, generating about 104 virions per infected cell. In humans, Ads generally cause only relatively mild, self-limiting illness in immunocompetent individuals. Ads have never been implicated as a cause of malignant disease in their natural host. The reader is referred to an excellent review by Shenk (5) for a more comprehensive discussion of the adenovirus. 1.2. Adenovirus Vectors Typically, Ads are modified into vectors by replacing the E1 region with the foreign DNA of interest. This modification serves two important purposes. First, deletion of E1 increases the cloning capacity to approx 5 kb. Second, it renders the vectors replication deficient, which is an important consideration with respect to safety for human gene therapy. These replication-deficient vectors can be propagated in E1-complementing cell lines such as 293 (14). The E3 region can also be deleted from the vector as it is not required for virus propagation in culture. The combination of E1 and E3 deletions results in a cloning capacity of approx 8 kb, a size that is more than adequate for most expression cassettes. 1.3. Overview of the Two-Plasmid Rescue System This chapter provides detailed protocols for construction of E1-substituted Ad vectors by site-specific recombination between two plasmids cotransfected into E1-complementing cells such as 293 (Fig. 2) (15–17). One of the plasmids used in this method contains the entire Ad5 genome except for certain key deletions. Essential features of this Ad genomic plasmid include an ITR junction, a deletion spanning the E1 region and packaging signal, a target sequence for site-specific recombination, and a cassette for expression of the site-specific recombinase. Inclusion of the recombinase expression cassette allows sitespecific recombination-mediated vector rescue to be performed in any

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Fig. 2. Construction of Ad vectors by Cre- or FLP-mediated site-specific recombination following cotransfection of 293 cells with an Ad genomic plasmid (see Fig. 3), and a shuttle plasmid (see Fig. 4). Ad and bacterial plasmid sequences are represented by thick and thin lines, respectively, and loxP or frt sites are represented by “ .”

E1-complementing cell. The recombinase expression cassette is not incorporated into the recombinant vector due to its location in the plasmid with respect to the recombinase target site (Fig. 2). The second plasmid, called a shuttle, contains an ITR junction, a packaging signal, a polylinker region for insertion of foreign sequences, and a target sequence for site-specific recombination. The ITR junctions serve as efficient origins of Ad DNA replication (18) so that following cotransfection into 293 cells, the plasmids can undergo Ad-mediated DNA replication. However, the deletion of the packaging signal renders the Ad genomic plasmid noninfectious. The presence of the ITR junction in the shuttle plasmid significantly increases the efficiency of vector rescue (16). Following cotransfection in 293 cells, site-specific recombination between the two plasmids results in the generation of a recombinant Ad vector, which can replicate and be packaged into infectious virions, resulting in plaques on the monolayer of 293 cells. Since neither plasmid alone is capable of producing infectious virus, only the desired recombinant vector is generated following


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cotransfection. Vector rescue can be achieved by either of two site-specific recombination systems with comparable high efficiencies: the bacteriophage P1 Cre/loxP system (15,16) or the yeast FLP/frt system (17). 2. Materials 2.1. Preparation of Plasmid DNA 1. Plasmid DNA: All plasmids described in this chapter and their sequences can be obtained from Microbix Biosystems (www.microbix.com). 2. Sterile Luria-Bertani (LB) broth (Lennox; Difco) and LB-agar plates supplemented with 50 μg/mL ampicillin. 3. Solution I: 10 mM EDTA, pH 8.0, 50 mM glucose, 25 mM Tris-HCl, pH 8.0, prepared from sterile stock solutions. 4. Solution II: 1% sodium dodecyl sulfate (SDS), 0.2 N NaOH, freshly prepared. 5. Solution III: 3 M potassium acetate, 11.5% glacial acetic acid, autoclave-sterilized. 6. Isopropanol. 7. TE: 10 mM Tris-HCl, pH 8.0, 1 mM EDTA pH 8.0, autoclave-sterilized. 8. Pronase stock solution: 20 mg/mL pronase in 10 mM Tris-HCl, pH 7.5. Preincubate at 56°C for 15 min followed by 37°C for 1 h. Aliquot and store at –20°C. 9. Pronase-SDS solution: 0.5 mg/mL pronase (above) in 0.5% SDS, 10 mM TrisHCl, pH 7.4, 10 mM EDTA, pH 8.0. 10. CsCl (biotechnology grade). 11. 10 mg/mL ethidium bromide.

2.1.1. Ad Genomic Plasmids A variety of Ad genomic plasmids are available for construction of vectors (Fig. 3). The plasmids pBHGloxE3Cre and pBHGfrtE3FLP are used to generate vectors bearing a wild-type E3 region by Cre-mediated and FLP-mediated recombination, respectively. The maximum foreign DNA insert that can be rescued into an E1-deleted vector with a wild-type E3 region is approx 5 kb owing to the size constraints of Ad (19). The plasmids pBHGloxΔE3(X1)Cre and pBHGfrtΔE3(X1)FLP have a 1864-bp deletion in the E3 region and thus permit rescue into vectors of foreign sequences up to approx 7.2 kb by Cremediated and FLP-mediated recombination, respectively. The plasmids pBHGloxΔE1,3Cre and pBHGfrtΔE1,3FLP have a 2653-bp deletion in the E3 region and permit rescue into vectors of foreign sequences up to approx 8 kb by Cre-mediated and FLP-mediated recombination, respectively. These latter two plasmids offer maximum cloning capacity, but vectors bearing this larger E3 deletion may grow slightly more slowly and result in lower yields (approx twofold) than vectors bearing the wild-type or smaller E3 deletion (F. L. Gra-

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Fig. 3. Ad genomic plasmids used for vector rescue by site-specific recombination in vivo. The plasmids pBHGloxE3Cre, pBHGloxΔE3(X1)Cre, and pBHGloxΔE1,3Cre are used to rescue vectors bearing a wild-type E3 region, a 1864-bp deletion or a 2653bp deletion of E3, respectively, by Cre-mediated recombination. The plasmids pBHGfrtE3FLP, pBHGfrtΔE3(X1)FLP, and pBHGfrtΔE1,3FLP are used to rescue vectors bearing a wild-type E3 region, a 1864-bp deletion, or a 2653-bp deletion of E3, respectively, by FLP-mediated recombination. The unique PacI restriction enzyme site in pBHGloxΔE1,3Cre, pBHGloxΔE3(X1)Cre, pBHGfrtΔE3(X1)FLP, and pBHGfrtΔE1,3FLP permit insertion of foreign sequences into the E3 deletion. Ad and bacterial plasmid sequences are represented by thick and thin lines, respectively, and loxP or frt sites are represented by “ .”


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ham, unpublished results). The presence of a unique PacI site in pBHGfrtΔE1,3FLP, pBHGloxΔE1,3Cre, pBHGloxΔE3(X1)Cre, and pBHGfrtΔE3(X1)FLP permits insertion of foreign sequences for rescue into the E3 deletion if desired (Fig. 3). The choice of which Ad genomic plasmid to use is dictated by the size of the foreign sequence to be rescued, whether a wild-type or a deleted E3 region is desired in the vector, and which site-specific recombination system is preferred/necessitated. 2.1.2. Shuttle Plasmids A variety of small shuttle plasmids are available for insertion of foreign sequences and rescue into Ad vectors by Cre- or FLP-mediated recombination (Fig. 4). The shuttle plasmids pDC311, pDC312, pDC511, and pDC512 are designed for the insertion of expression cassettes for rescue into vectors, the first two by Cre-mediated recombination and the last two by FLP-mediated recombination. The shuttle plasmids pDC315, pDC316, pDC515, and pDC516 are designed for the insertion of coding sequences for rescue into vectors, the first two by Cre-mediated recombination and the last two by FLP-mediated recombination. In these plasmids, the site of insertion is flanked by a murine cytomegalovirus (MCMV) immediate early promoter and the SV40 polyadenylation signal, thus permitting high-level transgene expression. The choice of which shuttle plasmid to use is dictated by whether expression from a strong viral promoter is desired, by the orientation of the polylinker, and by the site-specific recombination system desired for vector rescue. We have observed that higher expression levels are obtained when the transcription orientation of the transgene is in the same direction as E1 and that the MCMV immediate early promoter is stronger in most cell lines than its more commonly used human counterpart (20). 2.2. Cell Culture 1. Low-passage 293 cells (Microbix Biosystems). 2. 293N3S cells (Microbix Biosystems). 3. Complete medium: minimum essential medium (MEM; Gibco-BRL, cat. no. 61100) containing 10% fetal bovine serum (FBS) (heat inactivated), 100 U/mL penicillin/streptomycin, 2 mM L-glutamine, and 2.5 μg/mL fungizone. 4. Joklik’s modified-MEM (Gibco-BRL, cat. no. 22300) supplemented with 10% horse serum (heat inactivated). 5. Citric saline: 135 mM KCl, 15 mM sodium citrate, autoclave-sterilized.

2.3. Cotransfection 1. Monolayers of low-passage 293 cells at 80% confluency in 60-mm dishes. 2. HEPES-buffered saline (HBS): 21 mM HEPES,137 mM NaCl, 5 mM KCl, 0.7 mM Na2HPO4, 5.5 mM glucose, pH 7.1 (adjusted with NaOH), filter-sterilized. Store at 4°C in small aliquots in tightly sealed conical tubes.

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Fig. 4. Shuttle plasmids and their polylinker sequences used for vector rescue by in vivo site-specific recombination. The shuttle plasmids pDC311 (3276 bp), pDC312 (3288 bp), pD315 (3913 bp), and pDC316 (3913 bp) are used to rescue vectors by Cremediated recombination. The shuttle plasmids pDC511 (3277 bp), pDC512 (3277 bp), pDC515 (3957 bp), and pDC516 (3957 bp) are used to rescue vectors by FLP-mediated recombination. The plasmids pDC311, pDC312, pDC511, and pDC512 are used for insertion of expression cassettes (inserts with a promoter/enhancer and

First-Generation Adenoviral Vectors 3. 4. 5. 6.

7. 8. 9. 10. 11. 12.

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Salmon sperm DNA (2 μg/μL in TE). 2.5 M CaCl2, filter-sterilized. Complete medium (see Subheading 2.1.). 2× maintenance medium: 2× MEM (Gibco-BRL, cat. no. 61100) supplemented with 10% horse serum (heat inactivated), 200 U/mL penicillin/streptomycin, 4 mM L-glutamine, 5 μg/mL fungizone, and 0.2% yeast extract. 1% agarose solution, autoclave-sterilized. Store at room temperature and melt in a microwave oven prior to use. Ad genomic plasmid DNA (see Subheading 2.2.1.). Shuttle plasmid DNA with desired foreign sequence inserted (see Subheading 2.2.2.). Phosphate-buffered saline (PBS): 137 mM NaCl, 8.2 mM Na2HPO4, 1.5 mM KH2PO4, 2.7 mM KCl, autoclave-sterilized. PBS2+: PBS supplemented with 0.68 mM sterile MgCl2 and 0.5 mM sterile CaCl2. Glycerol, autoclave-sterilized.

2.4. Analysis of Recombinant Vectors 1. 2. 3. 4.

90% confluent 60-mm dishes of 293 cells. TE (see Subheading 2.1.). Complete medium (see Subheading 2.1.). Maintenance medium: MEM (Gibco-BRL, cat. no. 61100) containing 5% horse serum (heat inactivated), 100 U/mL penicillin/streptomycin, 2 mM L-glutamine, and 2.5 μg/mL fungizone. 5. PBS2+ (see Subheading 2.3.). 6. Pronase-SDS solution (see Subheading 2.1.).

2.5. Titration of Adenovirus 1. 2. 3. 4. 5.

80–90% confluent 60-mm dishes of 293 cells. PBS2+ (see Subheading 2.3.). 1% agarose solution (see Subheading 2.3.). 2× maintenance medium (see Subheading 2.3.). Glycerol, autoclave-sterilized.

2.6. Preparation of High-Titer Viral Stocks (Crude Lysate) 1. PBS2+ (see Subheading 2.3.). 2. Glycerol, autoclave-sterilized.

Fig. 4. Continued polyadenylation signal as well as coding sequence). The plasmids pDC315, pDC316, pDC515, and pDC516 bear a polylinker flanked by the murine cytomegalovirus immediate early promoter/enhancer and SV40 polyadenylation signal and are used for insertion of coding sequences (e.g., cDNAs).

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Specific materials, in addition to those above, are required for virus preparation from either 293 cells or 293N3S cells as listed below. 2.6.1. Preparation of High-Titer Viral Stocks (Crude Lysate) from Cells in Monolayer 1. 150-mm dishes of 80–90% confluent 293 cells. 2. Maintenance medium (see Subheading 2.4.).

2.6.2. Preparation of High-Titer Viral Stocks (Crude Lysate) from Cells in Suspension 1. 3–4 L 293N3S cells (Microbix Biosystems). 2. Joklik’s modified MEM supplemented with 10% horse serum (heat inactivated) (see Subheading 2.2.). 3. 1% sodium citrate. 4. Carnoy’s fixative: Add 25 mL glacial acetic acid to 75 mL methanol. 5. Orcein solution: Add 1 g orcein dye to 25 mL glacial acetic acid plus 25 mL dH2O and filter through Whatman no. 1 paper.

2.7. Purification of Adenovirus by CsCl Banding 1. 2. 3. 4.

10 and 100 mM Tris-HCl, pH 8.0, autoclave-sterilized. 5% sodium deoxycholate, filter-sterilize. 2 M MgCl2, autoclave-sterilized. DNAase I: 100 mg bovine pancreatic deoxyribosenuclease I in 10 mL of 20 mM Tris-HCl, pH7.4, 50 mM NaCl, 1 mM dithiothreitol, 0.1 mg/mL bovine serum albumin, 50% gyclerol. Aliquot and stored at –20°C). 5. CsCl solutions: Density (g/ml) 1.5 1.35 1.25

CsCl (g) 90.8 70.4 54.0

10 mM Tris-HCl, pH 8.0 (g) 109.2 129.6 146.0

Dissolve CsCl into 10 mM Tris-HCl, pH 8.0, solution in the amounts indicated above to achieve the desired density solution, and filter sterilize. Weigh 1.00 mL to confirm density. 6. Glycerol, autoclave-sterilized. 7. Beckman SW 41 Ti and SW50.1 rotor and ultraclear tubes. 8. Slide-A-Lyzer dialysis cassettes (Pierce).

2.8. Characterization of Adenoviral Vector Preparations 1. All materials listed in Subheading 2.5. 2. TE (see Subheading 2.1.). 3. 10 mM Tris-HCl, pH 8.0.


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4. 5. 6. 7. 8. 9.

10% SDS Pronase-SDS solution (see Subheading 2.1.) 3 M sodium acetate, pH 5.2, autoclave-sterilized. 95% and 70% ethanol. A549 cells. α-MEM (Gibco-BRL, cat. no. 12000) supplemented with 10% FBS (heat inactivated). 10. α-MEM supplemented with 5% horse serum (heat inactivated).

3. Methods Figure 5 presents an overview of the steps involved in the production of recombinant Ad vectors. Briefly, 293 cells are cotransfected with the Ad genomic plasmid and the shuttle plasmid. The recombinant vector, generated by site-specific recombination in vivo between the two plasmids, forms a plaque in the cell monolayer. The plaques are isolated, the virus is expanded, and the vector DNA is extracted for confirmation by restriction enzyme digestion. The vector is plaque-purified by titration, and a high-titer stock is generated. The vector is then purified by CsCl banding and characterized with respect to concentration, DNA structure, level of RCA contamination, and transgene expression. The remainder of this chapter provides detailed protocols for each of these steps. Although it is recommended that the steps outlined in Figure 5 be followed, acceptable alternatives, where applicable, are provided in Subheading 3.9. to expedite vector production. 3.1. Preparation of Plasmid DNA The foreign DNA of interest is inserted into an appropriate shuttle plasmid and transformed into E. coli by conventional molecular biology techniques. The following is a protocol for the preparation of high-quality plasmid DNA for cotransfection. 1. Inoculate 5 mL of LB supplemented with 50 μg/mL ampillicin with bacteria bearing the desired plasmid in the morning. Incubate culture at 37°C with shaking (see Note 1). 2. Inoculate 500 mL of LB supplemented with 50 μg/mL ampillicin with the above culture in the late afternoon. Incubate overnight at 37°C with shaking (see Note 2). 3. Transfer culture to a centrifuge bottle and pellet bacteria by spinning at 6000g for 10 min at 4°C. 4. Resuspend bacterial pellet in 40 mL of cold solution I so that no cell clumps are visible. 5. Add 80 mL of freshly prepared solution II, and mix thoroughly but gently by swirling. This should produce a relatively clear, viscous lysate.

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Fig. 5. Overview of the steps involved in rescue, propagation, purification, and characterization of Ad vectors. The recommended steps are indicated by thick arrows. Acceptable alternatives to expedite vector production are indicated by thin arrows (see Subheading 3.9.).


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6. Add 40 mL of cold solution III, mix thoroughly but gently by swirling, and incubate for 20 min on ice. A white precipitate should form, and the viscosity should be greatly reduced. 7. Add 10 mL of dH20, and centrifuge at 4°C for 10 min at 6000g. 8. Collect the supernatant by filtering it through two to three layers of cheesecloth into a centrifuge bottle. 9. Precipitate plasmid DNA by adding 100 mL (0.6 vol) of isopropanol, mix well, and incubate for 30 min at room temperature. 10. Pellet plasmid DNA by centrifuging at 4°C for 10 min at 6000g. 11. Pour off the supernatant and drain at room temperature for 15 min. Keeping the bottle upside down, wipe inside the rim with a clean KimWipe™ to remove all residual isopropanol. 12. Dissolve plasmid DNA pellet in 5 mL TE and transfer to 50-mL conical tube. 13. Add 2 mL pronase-SDS solution, mix well, and incubate for 30 min at 37°C. 14. Add 8.6 g CsCl, mix to dissolve completely, and incubate on ice for 30 min. 15. Centrifuge at maximum speed in a Beckman tabletop centrifuge for 30 min at 5°C. Slowly collect the supernatant using a 10-mL syringe and 16-gage needle, avoiding as much of the pellicle as possible. 16. Transfer to a Beckman VTi 65.1 ultracentrifuge tube. Add 25 μL of 10 mg/mL ethidium bromide and fill the tube with light parafin oil. Seal the tube and mix by inversion. 17. Centrifuge in a Beckman VTi 65.1 rotor at 55,000 rpm (288,000g) for 10–14 h at 14°C. 18. Remove tube and support it with a stand. The supercoiled plasmid DNA band should be the thicker, lower red band in the gradient, but it should not be at the very bottom of the tube. The upper red band (if present) is nicked plasmid or chromosomal DNA. Puncture the top of the tube to allow entry of air. Collect plasmid DNA through the side of the tube with a 3-mL syringe and 18-gage needle by puncturing the side of tube just below the band. (see Note 3). 19. Transfer plasmid DNA to a 15-mL polypropylene tube containing 5 mL isopropanol, which has been saturated with CsCl in TE, and mix immediately to extract the ethidium bromide into the solvent layer. Allow the phases to separate and remove the ethidium bromide-solvent (pink) layer. Repeat extraction until the solvent layer is completely colorless. 20. Add TE to bring the volume up to 4 mL, add 8 mL cold 95% ethanol, and mix by inversion to precipitate the DNA. 21. Centrifuge at top speed for 15 min to pellet DNA. Discard supernatant and wash pellet twice with 5 mL 70% ethanol. 22. Remove as much of the 70% ethanol as possible, allow the pellet to dry, and resuspend with an appropriate volume of TE. Ideally, the concentration should be 1–2 μg/μL. 23. Determine the plasmid DNA concentration by OD260, digest a sample with appropriate diagnostic restriction enzymes, and confirm the structure by agarose gel electrophoresis.

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3.2. Cell Culture Low-passage 293 cells maintained in 150-mm dishes, are split 1 to 2 or 1 to 3 when they reach approx 90% confluency (every 2–3 days). In general, for cotransfections, a confluent 150-mm dish of 293 cells is split into eight 60-mm dishes for use the next day (see Note 4). 1. Remove medium from 150-mm dish of 293 cells. 2. Rinse monolayer twice with 5 mL citric saline. 3. Remove citric saline from step 2, add 0.5 mL citric saline, and leave the dish at room temperature until cells start to round up and detach from the dish (no more than 15 min). 4. Tap the side of the dishes to detach all cells. 5. Resuspend cells with complete medium and distribute into new dishes.

293N3S are suspension-adapted 293 cells and can be used for large-scale vector production instead of 293 cells because of their greater ease of handling. 293N3S cells are grown in Joklik’s modified MEM supplemented with 10% horse serum (heat inactivated) and should be diluted 1 to 2 or 1 to 3 when the density reaches 5 × 105 cells/mL. All cell culture reagents should be prewarmed to 37°C prior to use. 3.3. Cotransfection Typically, a large number of plaques are generated by cotransfecting a single 60-mm dish of 293 cells with 2 μg of the shuttle plasmid and 2 μg of the Ad genomic plasmid by site-specific recombination (Table 1). However, a number of factors can influence the efficiency of vector rescue including the quality of the DNA, the efficiency of transfection, and especially the state of the 293 cells. Another important consideration is that the plaques be well isolated. Therefore, it is recommended that a range of DNA amounts be cotransfected to ensure that the vector is rescued and also that the plaques are well isolated. The infectious Ad genomic plasmid pFG140 (18) is used as a control for transfection efficiency and under optimal conditions should yield up to approx 100 plaques per 0.5 μg. Below is a typical protocol in which four 60-mm dish of 293 cells are cotransfected with 0.5, 2, and 5 μg of each plasmid (Fig. 6). 1. Label four 60-mm dishes “A,” four dishes “B,” four dishes “C,” and two dishes “D” and seed them with 293 cells to reach approx 80% confluency in 1–2 days for cotransfection. 2. In the late afternoon, 1 h prior to cotransfection, the medium from the 60-mm dishes of 293 cells is replaced with 5 mL of freshly prepared complete medium without washing. 3. Meanwhile, combine in a 50-mL conical tube 8 mL of HBS and 40 μl of salmon sperm DNA and vortex at maximum setting for 1 min.


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Fig. 6. Standard cotransfection protocol for Ad vector rescue by in vivo site-specific recombination.

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Table 1 Vector Rescue Efficiency by In Vivo Site-Specific Recombinationa Shuttle plasmid

Ad genomic plasmid

Average plaques/60-mmdish

pCA35loxΔITR

pBHGloxΔE1,3Cre pBHGloxΔE3(X1)Cre pBHGloxE3Cre pBHGfrtΔE1,3FLP pBHGfrtΔE3(X1)FLP pBHGfrtE3FLP pFG140 b

43 63 48 41 27 25 103

pCA35frtΔITR

60-mm dishes of 293 cells were cotransfected with 2 μg of each plasmid, and plaques were counted at 10 days post cotransfection. b 60-mm dishes of 293 cells were transfected with 0.5 μg of pFG140, and plaques were counted at 10 days post cotransfection. a

4. Aliquot 2 mL each of the above solution to three polystyrene tubes labeled “A,” “B,” and “C”and 1 mL into a fourth polystyrene tube labeled “D.” 5. To tube “A” add 2 μg of shuttle plasmid DNA and 2 μg of Ad genomic plasmid DNA. (This will result in 0.5 μg of each plasmid per dish.) To tube “B” add 8 μg of shuttle plasmid DNA and 8 μg of Ad genomic plasmid DNA (2 μg of each plasmid per dish). To tube “C” add 20 μg of shuttle plasmid DNA and 20 μg of Ad genomic plasmid DNA (5 μg of plasmid per dish). To tube “D” add 1 μg of pFG140 DNA. Mix each tube thoroughly but gently. 6. Add 100 μL of 2.5 M CaCl2 dropwise to tubes “A,” “B,” and “C” with gentle mixing. Add 50 μL of 2.5 M CaCl2 dropwise to tube “C” with gentle mixing. The solutions should become slightly cloudy. Incubate at room temperature for 30 min. 7. Apply 0.5 mL of the contents in tube “A” dropwise to the monolayer in each of the dishes labeled “A” without removing the medium. Do the same for tubes “B,” “C,” and “D”. Rock the dishes to distribute the precipitate evenly, and return to the incubator. 8. Next day, melt 1% agarose solution in a microwave oven and allow it to equilibrate to 45°C in a waterbath. Equilibrate 2× maintenance medium to 37°C. Once the two solutions have equilibrated to the desired temperature, prepare overlay solution by combining 70 ml of melted 1% agarose and 70 mL of 2× maintenance medium. 9. Remove the medium from the cotransfected dishes and add 10 mL of the overlay prepared in step 8 to each dish (see Note 5). 10. Allow the overlay to solidify at room temperature (10–15 min), and then return the dishes to the incubator. Plaques should begin to appear as early as 5 days post cotransfection and will continue to appear until about 12–14 days postcotransfection.


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11. Ten days post cotransfection, pick well-isolated plaques from the monolayer by punching out agar plugs with a sterile cotton-plugged Pasteur pipet attached to a rubber bulb (see Note 6). 12. Transfer the agar plugs into 0.5 mL PBS2+ supplemented with glycerol to 10% in a suitable vial. Vortex briefly and store at –70°C.

It is recommended that mock-transfected controls be included for comparison until the researcher gains familiarity with the appearance and morphology of Ad plaques. 3.4. Analysis of Recombinant Vectors Once plaques have been isolated, they are expanded for extraction of vector DNA for analysis and to yield a working vector stock as follows: 1. Seed 60-mm dishes of 293 cells (one per plaque) to reach approx 90% confluency on the day of use. 2. Thaw virus plaque picks and vortex briefly. Remove medium from 60-mm dishes of 293 cells and add 0.2 mL of the plaque pick. Adsorb for 1 h in the incubator, rocking the dishes every 10–15 min. 3. Following adsorption, add 5 mL of maintenance medium and return dishes to incubator until complete cytopathic effect (CPE) is observed (≥90% cells rounded up and detached from dish, usually 3–4 days post infection) (see Note 7). 4. Once complete CPE is reached, the dishes can be processed as follows: leave dishes undisturbed in a laminar flow hood for 20–30 min to allow cells in suspension to settle. Gently remove medium with a pipet, leaving the majority of the cell in the dish. Transfer the medium into a suitable vial, supplement with glycerol to 10%, and store at –70oC. The medium should contain a significant amount of virus (107–108 plaque-forming units [pfu]/mL) and can be used for plaque purification of the vector (see Subheading 3.5.) (or can be used in preliminary experiments or for further vector expansion, as described in Subheading 3.6.). 5. Add 0.5 mL pronase-SDS solution and incubate dishes at 37°C overnight. 6. Transfer lysate to a microfuge tube and add 1 mL 95% ethanol. Precipitate DNA by inverting the tube several times. 7. Pellet DNA by spinning in a microcentrifuge (maximum speed for 2 min) and wash pellet twice with 70% ethanol. Let the pellet dry and resuspend in an appropriate volume of TE (approx 50–100 μL). Dissolve DNA by heating at 65oC with occasional vortexing. 8. Digest 5–10 μL of the DNA with an appropriate restriction enzyme and analyze the DNA structure by ethidium bromide staining following agarose gel electrophoresis to verify the DNA structure of the recombinant virus is correct.

Once the DNA structure of the vector has been verified, it is purified by titration (see Subheading 3.5.).

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3.5. Titration of Adenovirus The procedure outlined below is used to plaque purify recombinant vectors and also to determine the concentration of vector stocks (see Note 8). 1. Seed 60-mm dishes of 293 cells to reach approx 80–90% confluency in 1–2 days for titration. 2. Prepare serial dilutions of the recombinant virus in PBS2+ (10-2–10-6 for samples prepared in Subheading 3.4. and 10-4–10-10 for samples prepared in Subheading 3.6. and 3.7.). 3. Remove medium from 60-mm dishes of 293 cells and infect with 0.2 mL of the diluted samples. Return dishes to the incubator and adsorb for 1 h, rocking the dishes every 10–15 min. 4. During the adsorption period, melt 1% agarose solution in a microwave oven and equilibrate to 45°C in a waterbath. Equilibrate 2× maintenance medium to 37°C. 5. Following 1-h adsorption, combine equal volumes of molten agarose solution with 2× maintenance medium, mix well, and gently overlay dishes with 10 mL (see Note 5). 6. Allow overlay to solidify for 10–15 min and return dishes to the incubator. 7. Plaques should start to appear about 4 days post infection and should be counted 12 days post infection. For isolation of recombinant virus by plaque purification, well-isolated plaques should be picked according to steps 11 and 12 of Subheading 3.3. around 10 days post infection. The plaque-purified vectors are expanded according to Subheading 3.4. and used as inoculum for the preparation of hightiter viral stocks (see Subheading 3.6.). 8. Determine the vector concentration in pfu/mL as follows: titer = (number of plaques)(dilution factor)/(infection volume) Calculate the titer from dishes bearing 20–70 plaques.

3.6. Preparation of High-Titer Viral Stocks (Crude Lysate) Because most of the virus remains associated with the infected cells until very late in infection (i.e., until the cells lyse), high-titer stocks can be prepared easily by concentrating infected 293 cells. The following protocol describes the production of high-titer virus preparations using either monolayers of 293 cells or suspension cultures of 293N3S cells. However, because of the greater ease of handling suspension cultures, 293N3S cells are preferable for the production of very large amounts of high-titer viral stocks. The following describes protocols for the preparation of crude lysates of high-titer vector stocks that are suitable for most experiments. Prior to the preparation of high-titer stocks, confirm that enough inoculum is available and if not, prepare an intermediatescale virus stock by infecting two to three 150-mm dishes of 293 cells.


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3.6.1. Preparation of High-Titer Viral Stocks (Crude Lysate) from Cells in Monolayer 1. Set up 150-mm dishes of 293 cells to be 80–90% confluent at the time of infection. The number of dishes is dictated by the amount of vector desired (20–30 dishes can be easily handled). 2. Dilute virus sample prepared as in Subheading 3.5., step 7, 1:8 with PBS2+. 3. Remove medium from the 293 cells and add 1 mL of the diluted virus sample prepared in step 2 to each 150-mm dish of cells (MOI of 1–10 pfu/cell). 4. Adsorb for 1 h in the incubator, rocking the dishes every 10–15 min. Following adsorption, add 25 mL maintaince medium and return dishes to the incubator. Examine daily for signs of cytopathic effect. 5. When cytopathic effect is nearly complete, i.e., most cells rounded but not yet detached, harvest by scraping the cells into the medium and centrifuging the cell suspension at 800g for 15 min. 6. Discard the supernatant and resuspend the cell pellet in 2 mL PBS2+ + 10% glycerol per 150-mm dish infected. Freeze (–70°C) and thaw the crude virus stock prior to characterization of the vector (see Subheading 3.8.). Store aliquots at –70°C.

3.6.2. Preparation of High-Titer Viral Stocks (Crude Lysate) from Cells in Suspension 1. Grow 293N3S cells to a density of 2–4 × 105 cells/mL in 4 L complete Joklik’s modified MEM supplemented with 10% horse serum. Centrifuge cell suspension at 750g for 20 min, saving half of the conditioned medium. Resuspend the cell pellet in 0.1 vol fresh medium, and transfer to a sterile 500-mL bottle containing a sterile stir bar. 2. Add virus at an MOI of 10–20 pfu/cell and stir gently at 37°C. After 1 h, return the cells to the 4-L spinner flask and bring to the original volume using 50% conditioned medium and 50% fresh medium. Continue stirring at 37°C. 3. Monitor infection daily by inclusion body staining as follows: a. Remove a 5-mL aliquot from the infected spinner culture. Spin for 10 min at 750g and resuspend the cell pellet in 0.5 mL of 1% sodium citrate. b. Incubate at room temperature for 10 min; then add 0.5 mL Carnoy’s fixative and fix for 10 min at room temperature. c. Add 2 mL Carnoy’s fixative, spin for 10 min at 750g, aspirate, and resuspend the pellet in a few drops of Carnoy’s fixative. Add 1 drop of fixed cells to a slide and air-dry for about 10 min; then add 1 drop orcein solution and a cover slip and examine using a microscope. Inclusion bodies appear as densely staining nuclear structures resulting from accumulation of large amounts of virus and viral products at late times post infection. A negative control should be included in initial tests. 4. When inclusion bodies are visible in 80–90% of the cells (1 1/2–2 1/2 days depending on the input MOI), harvest by centrifugation at 750g for 20 min in sterile 1-L bottles. Combine pellets in a small volume of medium, and spin again.

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5. Discard supernatant and resuspend pellet in 20 mL PBS2+ supplemented with 10% glycerol. Freeze (–70°C)- thaw, then aliquot, store at –70°C and characterize vector as described in Subheading 3.8.

3.7. Purification of Adenovirus by CsCl banding Many experimental studies can be carried out using virus in the form of crude infected cell lysates prepared as described in Subheading 3.6. However, for some experiments, particularly for animal work, it is usually desirable to use purified virus. The following protocol describes a method for purifying vectors by CsCl banding obtained from 4 L of infected 293N3S cells, or 30 × 150-mm dishes of 293 cells. 1. Prepare crude cell lysate from infected cells as follows: a. For 30 × 150-mm dishes prepared as in Subheading 3.6.1.: When complete CPE is evident, scrape the cells into the medium, transfer the cell suspension to a centrifuge bottle, and spin for 10 min at 750g. Resuspend cell pellet in 15 mL 0.1 M Tris-HCl, pH 8.0. Sample can be stored at –70°C. b. For 3-L spinner cultures prepared as in Subheading 3.6.2.: When inclusion bodies are visible in 80–90% of the cells, harvest cells by centrifugation at 750g for 20 min in sterile bottles. Resuspend pellet in 15 mL 0.1 M Tris-HCl, pH 8.0. Samples can be stored at –70°C. 2. Thaw sample and add 1.5 mL 5% Na deoxycholate for each 15 mL of cell lysate. Mix well and incubate at room temperature for 30 min. This results in a highly viscous suspension. 3. Add 150 μL 2 M MgCl2 and 75 μL DNase I solution for each 15 mL of cell lysate, mix well, and incubate at 37°C for 60 min, mixing every 10 min. The viscosity should be reduced significantly. 4. Spin at 3000g for 15 min at 5°C in the Beckman tabletop centrifuge. 5. Meanwhile, prepare CsCl step gradients (one SW 41 Ti ultraclear tube for each 5 mL of sample): Add 0.5 mL of 1.5 g/mL solution to each tube. Gently overlay with 3.0 mL of 1.35 g/mL solution. Gently overlay this with 3.0 mL of 1.25 g/mL solution. 6. Apply 5 mL of supernatant from step 4 to the top of each gradient. If necessary, top up tubes with 0.1 M Tris-HCl, pH 8. 7. Spin at 35,000 rpm in a Beckman SW 41 Ti rotor (151,000g) at 10°C, for 1 h. 8. Collect virus band (should be at 1.25 d/1.35 d interface) with a needle and syringe by piercing the side of the tube. The volume collected is unimportant at this stage, so try to recover as much of the virus band as possible. If more than one tube was used, pool virus bands into a Beckman SW 50.1 ultraclear tube. 9. Top up tubes with 1.35 g/mL CsCl solution if necessary and centrifuge in a SW50.1 rotor at 35,000 rpm (115,000g), 4°C, for 16–20 h. 10. To collect the virus band, puncture the side of the tube just below the virus band


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with a needle and syringe. Collect the virus band in the smallest volume possible and transfer to a Slide-A-Lyzer dialysis cassette. Dialyze at 4°C against three changes of 500 mL 10 mM Tris-HCl, pH 8.0, for at least 24 h total. 11. After dialysis, transfer the virus to a suitable vial and add sterile glycerol to a final concentration of 10%. Store the purified virus at –70°C in small aliquots.

3.8. Characterization of Adenoviral Vector Preparations Before the recombinant vector is used for experimentation, several basic characterizations should be performed: 1) the concentration should be determined; 2) the DNA structure should be confirmed; and 3) the presence and level of RCA should be ascertained. The concentration in pfu/mL is determined by titration on 293 cells as described in Subheading 3.5. The concentration of virus particles, based on DNA content at OD260, can also be determined spectrophotometrically as follows: 1. Dilute (usually 20-fold) purifed virus with TE supplemented with SDS to 0.1%. Set up blank the same except add virus storage buffer (10 mM Tris-HCl, pH 8.0, supplemented with glycerol to 10%) instead of virus. 2. Incubate for 10 min at 56°C. 3. Vortex sample briefly. 4. Determine OD260. 5. Calculate the number of particles/mL, based on the extinction coefficient of wildtype Ad as determined by Maizel et al. (21) as follows: (OD260)(dilution factor)(1.1 × 1012)

The DNA structure of the recombinant vector should be confirmed following large scale preparation. Virion DNA can be extracted from CsCl banded virus for analysis as follows: 1. Add an appropriate volume (approx 25 μL depending on the concentration of the virus) of the purified virus to pronase-SDS solution to a final volume of 0.4 mL and incubate overnight at 37°C to lyse the virions and digest virion proteins. 2. Precipitate virion DNA by adding 1/10 vol 3 M sodium acetate, pH 5.2, and 2.5 vol 95% ethanol and incubate at –20°C for 15–30 min. 3. Spin in microcentrifuge for 10–15 min at maximum speed. 4. Discard supernatant and wash DNA pellet twice with 70% ethanol. 5. Dry DNA pellet and resuspend in an appropriate volume of TE.

For crude preparations, viral DNA can be extracted following infection of 293 cells as described in Subheading 3.4. A sample of the vector DNA is digested with the appropriate diagnostic restriction enzyme(s), and the structure of the DNA is analyzed by agarose gel electrophoresis.

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293 cells contain nts 1–4344 bp of Ad5 DNA (22) with consequent homology flanking the expression cassette of most first-generation vectors. Therefore, the possibility exists that homologous recombination between the Ad vector and the Ad sequences present in 293 cells may result in the formation of E1+ replication-competent Ad (RCA) (see Note 9). Thus, it is important to determine whether the vector preparations are contaminated with RCA and if so, at what level. A non-E1-complementing cell line, such as A549, can be used for this purpose since it supports replication of RCA but not the E1-deleted Ad vector. The protocol is as follows: 1. Seed two 60-mm dishes and one 150-mm dish of A549 cells in α-MEM supplemented with 10% FBS for each vector preparation to be tested 2. When the monolayers are 80–90% confluent, remove the medium and infect one 60-mm dish with 106 pfu and the other 60-mm dish with 107 pfu. (Make up the volume of the inoculum to 0.2 mL with PBS++). Infect the 150 mm dish with 108 pfu (make up the volume of the inoculum with 1 mL PBS2+.) Adsorb for 1 h in the incubator, rocking the dishes every 10–15 min. 3. Following adsorption, add 5 and 25 mL of α-MEM supplemented with 10% horse serum to each 60-mm dish and 150-mm dish, respectively, and return dishes to incubator. 4. Infection of A549 cells with high-titer Ad, even in the absence of RCA, will frequently result in complete CPE of the initial A549 monolayer because of toxicity of viral proteins in the inoculum and multiplicity-dependent “leaky” viral replication. Harvest the monolayers 7 days post infection or when complete CPE is observed, whichever occurs first. Harvest the monolayer by scraping the cells into the medium. Transfer 3 mL of the lysate into a suitable vial, supplement with glycerol to 10%, and store at –70°C. 5. Set up four 150-mm dishes of A549 cells, one for each of the lysates collected in step 4 and one control. 6. When the monolayers reach 80–90% confluency, infect one dish each with 1 mL of the 106, 107, and 108 lysates collected in step 4. “Infect” the control dish with 1 mL of PBS2+. Adsorb for 1 h in the incubator, rocking the dishes every 10–15 min. 7. Following adsorption, add 25 mL of α-MEM supplemented with 10% horse serum to each dish, and return dishes to incubator. 8. Replace the medium every 5 days if necessary. 9. Observe monolayers daily for signs of CPE by comparing the infected dishes with the control dish. If the infected dishes are indistinguishable from the control dish (no CPE) 21 days post infection, then the lysate collected at step 4 was free of RCA and thus, the original aliquot of the vector preparation used in step 2 was also RCA free (or below the limits of detection). This provides an estimate of the level of RCA in the vector stock (e.g., 1014 rAAV particles per vector preparation. 1.3. Vector Purification A significant advance in rAAV vector technology has been the recent development of refined chromatography purification methods that render traditional isopycnic CsCl gradient purification obsolete (10–12). Importantly, vector purity, biological potency, and process throughput are all increased using these chromatographic methods. We have achieved large-scale (≥1 L) vector purification from clarified cell lysates in 5000 rAAV particles/cell). A schematic of the cell isolation process is shown in Figure 3. 3.1.1. Generation of rAAV Producer Plasmid (pTP) Containing the Desired Transgene (cDNA) 1. Clone the desired cDNA into rAAV producer plasmid pTP-D6deltaNot using the unique NotI restriction sites (Fig. 2). This places the cDNA downstream of the

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Fig. 3. Stable rAAV producer cell line screening strategy. HeLa cells are initially transfected with a functional pTP producer plasmid, and the resulting neomycin-resistant cell colonies are picked into 96-well plates. Subsequently, a test plate is adenovirus infected to induce rAAV production. Cells producing high levels of rAAV are identified using a high-throughput dot-blot hybridization protocol with a probe specific to the rAAV genome. The top 5 producer lines are expanded for midscale rAAV screening, whereby rAAV from each line is purified by heparin affinity chromatography. The yield of purified rAAV particles from each line is quantified using real-time PCR to determine the rAAV particles per cell.

2.

3.

4. 5.

immediate early cytomegalovirus (IE CMV) promoter and between the AAV ITRs. Transform DH5-alpha E. coli and screen 40 ampicillin-resistant colonies by size using a supercoiled quick screen (see Note 1). Usually 10% of colonies contain the desired cDNA insert. Check AAV ITR integrity by restriction enzyme digestion with SmaI and MscI, which cut within the ITRs, and a second restriction enzyme digestion to orient the cDNA sequence 5'–3' relative to the promoter (see Note 2). Select two putative clones, and transfect plasmid pTP DNA into HeLa cells using Superfect Transfection Reagent (see Subheading 3.1.2.). Two days post transfection, confirm transgene expression by either immunofluorescence or Western blot analysis on the transfected cell lysate.

Adeno-Associated Virus Vectors

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3.1.2. Producer Cell Line Generation Using Superfect Transfection Reagent 1. Once a functional producer plasmid clone is identified, the isolation of stable cell lines is begun by seeding 2 × 105 low-passage HeLa cells into a 6-well plate in DMEM media. 2. The next day, dilute 2 μg of supercoiled producer plasmid DNA (dissolved in TE, pH 7.4) with HBSS in a total volume of 100 μL in a 1.5-mL microfuge tube. Mix and spin down. 3. Add 10 μL of SuperFect Reagent to the DNA solution. Mix by pipeting up and down several times, and incubate the mixture at room temperature for 10 min (see Note 3). 4. While the transfection mixture is incubating, remove growth media from HeLa cells and wash cells once with 2 mL of PBS. 5. Add 1 mL of DMEM media (including serum and antibiotics) to the transfection mixture, pipet up and down 2 times, and immediately add the mixture over the entire HeLa cell well in a dropwise manner. Incubate for 2 h at 37oC in a 5% CO2 incubator. 6. Aspirate media from the cells, wash 2× with PBS, and then add 2 mL of DMEM containing serum and antibiotics. Incubate overnight. 7. The next day, trypsinize transfected cells and plate in 100-mm tissue culture dishes in 10 mL of media at the following dilutions: 5 dishes at 5 × 103 cells, and 5 dishes at 7.5 × 103 cells, 5 dishes at 104 cells. Move dishes gently from side to side to distribute cells evenly. 8. After 2 days, aspirate cell media and replace with DMEM media supplemented with 700 μg/mL Geneticin (G418). 9. Continue incubating cells for 6–8 days in selective media until cell colonies appear (see Note 4). 10. When colonies are 2–3 mm in diameter, aspirate selective media from cells and wash with 10 mL of HBSS to remove cell debris. Add 8 mL of fresh selective media to dishes, and with a P-1000 pipetman (containing a sterile filter tip) depress the plunger and place the pipet tip over a single colony. Rotate the pipet to loosen cells and slowly release pressure on plunger to aspirate cells into tip along with 200 μL of media. Transfer cells into a single well of a 96-well plate. Pick 2 × 96-well plates in this manner. 11. Incubate cells in 96-well plates for approximately 4–6 days until 50% of wells are confluent (see Note 5). 12. Using a multichannel pipet, remove media and trypsinize cells in 20 μL volume. Add 150 μL of selective media, and resuspend cells well by pipeting up and down several times. Place 30 μL of the cell suspension into a 96-well “master plate” containing 150 μL of fresh selective media. Place 100 μL of the cell suspension into a separate 96-well “test plate” containing 100 μL of fresh selective media. Incubate both sets of plates at 37°C. 13. After overnight incubation of the test plates, aspirate media using a multichannel pipet, and add 100 μL of 2% DMEM containing 106 pfu of adenovirus 5 per well.

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14. Incubate test plates at 37°C for 36 h. Then carefully remove media (not detaching rounded cells) and add 100 μL of DNase digestion buffer to each well (see Note 6). Incubate at 37°C for 30 min. 15. Add 10 μL of denaturation buffer to each well and incubate at 65°C for 30 min. 16. Transfer cell lysates to a dot-blot apparatus on positively charged nylon membrane prewetted in 2× SSC. Apply lysate to apparatus and rinse wells with 100 μL of 0.4 M NaOH. 17. Remove nylon membrane, rinse twice with 2× SSC for 5 min, and allow membrane to air-dry for 15 min. Crosslink DNA to membrane using a UV crosslinker apparatus. 18. Hybridize membrane using a digoxigenin (or radioactive) labeled DNA probe specific for the transgene. Detect hybridization by chemiluminescence and expose to X-ray film. 19. Expand from master plate the 10 individual cell clones exhibiting the strongest hybridization and proceed to the midscale screen (see Note 7).

3.1.2. Midscale Production Screen 1. Expand putative rAAV producer cells until sufficient cells are present to seed three T-175 tissue culture flasks at a density of 6 × 106 cells/flask in DMEM media containing 2% FBS. 2. The next day, dilute an adenovirus stock in HBSS to a concentration of 2 × 108 pfu/mL and add 1 mL/flask. 3. Harvest cells at maximum complete cytopathic effect (CPE; all cells rounded with 10% floating), which is usually 48 h post infection. The cells should detach easily from the flask with a gentle tap. Pellet cells in a tabletop centrifuge at 2000 rpm (1000g) for 10 min at 4°C. 4. Resuspend the cell pellet in 6 mL of TMN. 5. Add deoxycholic acid to a final concentration of 0.5% and mix the lysate well (do not vortex). 6. Add Benzonase nuclease to a final concentration of 50 U/mL, mix, and incubate the lysate at 37°C for 30 min with intermittent mixing every 10 min to ensure complete cell lysis. 7. Clarify the lysate at 3500 rpm (2000g) for 30 min at 4°C to remove debris. Transfer the clarified lysate to a new 50-mL conical tube, and heat-inactivate adenovirus at 56°C for 30 min with intermittent vortexing every 10 min. 8. Quick freeze in a dry ice/ethanol bath and store at –20°C overnight (see Note 8). 9. After thawing, remove the floculent precipitate by centrifugation at 3500 rpm (2000g) for 30 min at 4°C. Filter the supernatant through a 1.2-μm syringe filter. 10. Purify small-scale vector preparation by heparin sulfate column chromatography (see Subheading 3.2.). 11. Analyze small-scale preparations by quantitative PCR to derive the DNase-resistant vector genomes per cell (see Subheading 3.3.1.). Calculate the particle per cell yield for each cell line. The optimal cell line should produce >5000 rAAV vector particles per cell.


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12. Expand the optimal producer cell line (in the presence of Geneticin) for largescale rAAV vector production (see Note 9).

3.2. Vector Purification 3.2.1. Cell Lysate Preparation and Column Chromatography rAAV-containing cell lysates for heparin column chromatography are easily prepared by detergent lysis, followed by the addition of an endonuclease to reduce lysate viscosity. Finally, the lysate is filtered through a 1-μm serum filter prior to column application. 1. Resuspend rAAV producer cells in TMN at a cell density of 5 × 106 cells/mL. Add deoxycholic acid and Benzonase to a final concentration of 0.5% and 50 U/ mL, respectively, and incubate for 30 min at 37°C with intermittent mixing. 2. Remove cellular debris by tabletop centrifugation at 3500 rpm (2000g) for 15 min at 4°C. Heat the clarified lysate to 56°C for 45 min to inactivate adenovirus and then freeze at –20°C overnight. 3. Thaw the lysate at 37°C and remove the floculent precipitate by centrifugation (2000g). 4. Filter the supernatant through a 1-μm serum capsule filter unit using a peristaltic pump at a flow rate of 10 mL/min. The cell lysate is ready for column application. 5. Connect a POROS HE20/M heparin column (1.7-mL bed volume) to a Biocad Sprint HPLC system (Applied Biosystems) or similar FPLC/HPLC system. 6. Equilibrate the column with 20 mL of equilibration buffer at a flow rate of 5 mL/ min. 7. Apply the clarified cell lysate (≤1.2 L) to the column at a flow rate of 3–5 mL/ min at ambient temperature using the internal Biocad system pumps. The system back pressure should not be allowed to exceed 800 psi, and lysate conductivity should be between 12 and 16 mS. 8. After sample loading, the column is washed with 60 mL of equilibration buffer at 3 mL/min. The A280 should return to baseline (≥0.005). 9. Elute rAAV by application of a linear NaCl gradient from 0.1 to 1 M (pH 8.0) at a flow rate of 3 mL/min over 20 column volumes (approx 34 mL). Collect 1-mL gradient fractions, with the single dominant protein peak eluting at approx 0.35 M NaCl. 10. To determine peak virus containing fractions, run a small aliquot (20 μL) of individual fractions on a 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gel followed by fluorescent staining (SYPRO-Orange). Identify those fractions that contain the highest levels of the three AAV capsid proteins (87-kDa VP1, 73-kDa VP2, and 61-kDa VP3). 11. Pool the peak virus-containing fractions (typically three) and dialyze against three changes of 20 mM Tris-HCl, pH 8.0, 2 mM MgCl2, 150 mM NaCl, and store in aliquots at –80°C in 5% glycerol (see Note 10).

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12. Determine rAAV vector yield using the titration methods detailed in Subheading 3.3. 13. Clean heparin column with 10 mM Tris-HCl (pH 8.0), 2.4 M NaCl at a flow rate of 5 mL/min followed by column equilibration with 20 mL of equilibration buffer prior to storage at 4°C (see Note 11).

3.3. Vector Quantitation 3.3.1. Quantitation of DNase-Resistant Vector Genomes In this section we describe a rapid, reproducible, and sensitive PCR-based method to measure DNase-resistant rAAV particles (DRPs). The DRP Taqman assay is essentially a modified dot-blot protocol whereby purified rAAV is serially diluted and sequentially digested with DNase I and proteinase K. A portion of the treated sample is then subjected to quantitative PCR analysis using the PE Applied Biosystems Prism 7700 sequence detector system (15,16). Comparison with a plasmid standard curve (using system software) allows accurate quantitation of the initial vector genome copy number. 1. Prepare 10-3, 10-4, and 10-5 serial dilutions of a rAAV viral stock in 1× PCR buffer. 2. Digest 100 μL of each rAAV serial dilution with 1 μL DNase I (350 U) for 30 min at 37°C (see Note 12). 3. Place a second 100-μL aliquot of the rAAV serial dilutions into separate microfuge tubes and maintain at 4°C. These serve as minus DNase I control samples. 4. After DNase digestion, add 10 μg of proteinase K (1 μL) to all samples and incubate at 50°C for 1 h. 5. Inactivate the proteinase K by a 20-min incubation at 95°C. 6. Add 2.5 μL of the treated rAAV vector dilutions to 22.5 μL of a standard 1X Taqman PCR master mix (PE Applied Biosystems) that contains the appropriate Taqman primers and probe sequences at their working concentrations to a 96well/tube Taqman PCR plate (see Note 13). 7. Concurrently, set up a DNA plasmid standard curve in triplicate using 102–106 AAV genome equivalents. To prepare a plasmid DNA standard for Taqman PCR, first accurately determine the plasmid DNA concentration by using a DNA-specific fluorescent stain (PicoGreen DNA Quantitation Kit; Molecular Probes). 8. Next, prepare a plasmid stock of 1010 copies/mL in TE and aliquot at 50 μL/tube. Store these aliquots at –20°C and use this stock to prepare 10-fold serial dilutions that will allow quantitation of between 5 × 101 and 5 × 106 plasmid molecules per Taqman reaction (see Note 14). 9. Perform a standard 40-cycle Taqman PCR amplification (50oC, 2 min, 1 cycle; 95°C, 10 min, 1 cycle; 95°C, 15 s, 60°C, 1 min, 40 cycles) using the Taqman 7700 PCR Sequence Detector (see Note 15).


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10. Using the system software, calculate the initial vector particle titer by comparing the amplification profile of the sample unknowns with the plasmid standard curve. The final titer is derived by multiplying the vector particle value by the dilution factor and then by 400 to derive a titer per mL. An example of a typical amplification profile is shown in the bottom left of Figure 3 (see Note 16).

3.3.2. Infectious rAAV Titration Using Quantitative PCR A second assay, developed for infectious rAAV titration, also uses a quantitative PCR approach. We have previously demonstrated the utility of a stable rep-cap-expressing HeLa cell line (C12) for replication-based rAAV titration (12,17). The assay is based on the ability of rAAV to replicate in C12 cells following coinfection with adenovirus. Using quantitative PCR, an end-point titer is generated based on the highest stock dilution that results in detectable rAAV vector genome amplification when compared with input vector (no adenovirus). The detection of rAAV replication at an end-point dilution could therefore be used to derive an infectious end-point titer (TCID50). At 36 h post infection, total cellular DNA is isolated from each infected well and subjected to quantitative PCR. Because of the extreme sensitivity of PCR-based methods, low levels of rAAV input DNA are amplified in the absence of adenovirus infection. However, at some dilutional end point, the input rAAV vector genomes will become titratable and thus undetectable by PCR, whereas cells infected by rAAV (in the presence of adenovirus) will replicate and result in an increase of ≥10-fold in the rAAV vector genome levels over input. 1. Seed two 24-well plates with 7 × 104 C12 cells/well in DMEM media. One plate will be adenovirus infected, and the other plate will serve as a control for input virus. 2. The next day, prepare 10-fold serial dilutions of the rAAV stock from 10-7 to 1012 using DMEM media containing 2% FBS. 3. Working with the minus Ad5 plate first, aspirate the media from the plate and infect cells with 0.5 mL of each viral dilution (6 wells total). 4. Aspirate the media from the adenovirus (+) plate. Starting with the highest dilution, infect 4 wells with 0.5 mL from each viral dilution (24 wells total). 5. Add 100 μL of DMEM media (2% FBS) containing 3 x 106 pfu of adenovirus type 5 to each well of the adenovirus (+) plate. 6. As a negative control, place 0.5 mL of 2% FBS DMEM on C12 cells alone. 7. After 36 h of incubation, the cells are ready for DNA isolation using a QIAamp Blood Isolation Kit-250. Starting with the adenovirus (-) plate, aspirate the media from the wells, and add 200 μL of 1× PBS to each well. 8. Add 25 μL of Qiagen Proteinase K and 200 μL of buffer AL. Gently rock the plate to ensure complete lysis. 9. Transfer the lysate from each well into a 1.5-mL microfuge tube, and incubate at 70°C for 10 min.

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10. Add 210 μL of 100% ethanol to each tube and vortex. Load DNA/ethanol mixture onto DNA spin columns that are hooked up to a Qiagen vacuum manifold. Allow the DNA/ethanol to enter the column completely, then wash with 500 μL of buffer Qiagen wash buffer (AW), and repeat. 11. Transfer each spin column to a new 1.5-mL microfuge tube, and elute DNA by the addition of 100 μL of buffer Qiagen elution buffer (AE) preheated to 70°C. Wait 1 min and then spin at 8000 rpm (6000g) for 1 min. Store DNA at 4°C prior to use. 12. Repeat steps 7–11 for adenovirus-infected samples. 13. Prepare the Taqman 1× master mix by adding the appropriate concentrations of primers and probe specific for your transgene or promoter to the supplied 2× Taqman master mix. 14. Add 22.5 μL of the Taqman master mix to each tube of the 96-tube/plate. Add 2.5 μL of the DNA sample (approx 500 ng) to each well and cap wells (see Note 17). 15. Perform a standard 40-cycle Taqman amplification on the Taqman 7700 Sequence Detector. 16. A standard curve is not necessary for this assay, although 105 plasmid targets should be run to serve as a positive control for the Taqman PCR reaction. 17. To determine an end-point infectious titer for the rAAV preparation, compare the amplification curve for each adenovirus-infected well with the input amplification profile at that particular dilution of the minus adenovirus sample. A cycle threshold difference of 3 or greater is indicative of input rAAV viral replication, and the well is scored positive. After scoring the wells, calculate a TCID50 endpoint titer using the Reed-Muench formula (see Note 18).

4. Notes 1. Because of possible plasmid instability, grow all bacteria harboring AAV ITRcontaining plasmids at 32°C. Rapid analysis of potential recombinant clones can be accomplished by screening the bacterial colonies by plasmid size using a supercoiled DNA plasmid ladder (Gibco-BRL). 2. ITR sequences can spontaneously rearrange or delete upon passage into bacteria. Therefore, all ITR-containing clones should be digested with SmaI and MscI, both of which cut within the ITRs. 3. We have used other transfection compounds (dioleoyl-trimethyl ammonium propane [DOTAP], Effectene, and CaPO4) with similar results. 4. Selective media should be changed every 4–5 days depending on accumulation of cellular debris. 5. The cells will grow at different rates; in general, 25% of cells are fast growing, 40% are medium growing, 25% are slow growing, and 10% will die when transferred. 6. The DNase treatment is optional and can be omitted. Inclusion of this step helps to reduce the number of putative rAAV vector-producing cell lines. 7. Typically, 10 cell lines are expanded and ≥107 cells from each are frozen (90% FBS + 10% dimethyl sulfoxide [DMSO]) and stored in liquid N2. The top five lines are expanded for midscale screening.


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8. Freezing of the lysate results in cellular protein precipitation that greatly increases the purity of the rAAV after column chromatography; therefore this step should not be omitted. 9. We have achieved large-scale producer cell growth (≥1010) using the Corning Cell Cube; alternatively, cells can be grown in T175 tissue culture flasks (100– 400). One to 3 days after seeding, cells are adenovirus infected at a multiplicity of infection (MOI) = 100. Harvest cells at maximum adenovirus CPE. Cell viability should be ≥80%. 10. We have found the Pierce Slide-a-Lyzer dialysis cassettes ideal for buffer exchange. 11. Column life is approximately 10 L of clarified lysate. We pack our own heparin columns using an Applied Biosystems packing device as instructed by the manufacturer. To extend the life of the column, more vigorous cleaning regimens can be used. We have found that a 0–100% isopropanol gradient or 0.5 N NaOH treatment (20–40 mL total volume) is useful to remove bound lipids and lipoproteins from the column. 12. DNase digestion, proteinase K incubation, and inactivation can all be conveniently performed in a preprogrammed PCR thermocycler. 13. Taqman PCR primers and probe sequences are identified using proprietary PE Applied Biosystems software. Working concentrations of the primers and probe are determined empirically using a plasmid containing the transgene sequence. 14. When calculating virus DRPs, remember that plasmid DNA is double-stranded, so 5 × 101 plasmid copies correspond to 102 genome copies of rAAV. 15. The Taqman 7700 is a 96-well thermocycler that utilizes a laser optic system, which provides periodic excitation to each well of the thermocycler. The fluorescence signal is generated by the PCR amplification process and occurs as a result of the 5'-3' nuclease activity of Taq polymerase. Fluorescence is achieved by the use of a dual-labeled (5' and 3' ends) fluorogenic oligonucleotide (referred to as the probe) that anneals specifically to the amplified PCR product. When the two fluorochromes are in physical proximity (connected by the oligonucleotide), the laser-excited fluorescent signal from the 5' reporter fluorescein is quenched (absorbed) by the 3' fluor. During the elongation phase of the PCR cycle, Taq polymerase degrades the annealed oligonucleotide, resulting in the release of the reporter fluorochrome into the medium and a consequent increase in reporter dye fluorescence. The increase in the reporter dye fluorescence is proportional to the number of PCR cycles. It is important to always perform replicates of 3 for each sample or standard. Also run three PCR reactions with no template (NTC) to control for reagent contamination. NTC reactions should fail to amplify, which results in a threshold cycle (CT) ≥ 39. 16. A normalized fluorescence value (ΔRn) is calculated by the system software and reflects the change in reporter fluorescence over time. ΔRn is plotted as a function of cycle progression; the first cycle that is above background fluorescence is defined as the threshold cycle (CT). A plot of the input plasmid copy number versus the CT value yields a standard curve with a dynamic range of ≥5 orders of

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magnitude. Routine detection of plasmid target input DNA is typically between 10 and 106 molecules per reaction 17. All samples should be run in duplicate; cells alone and adenovirus-infected C12 cells should also be run concurrently with NTC samples. All negative control samples should yield CT ≥ 39. 18. To standardize this titration method, positive sample amplification (plus adenovirus) was defined as possessing an average CT value (two replicates) that exceeded the corresponding minus adenovirus control sample by three or more PCR cycles (ΔCT ≥ 3). Based on numerous plasmid DNA amplification profiles, a 3–4 cycle differential represents an approximately 10-fold difference in starting template concentration.

References 1. Grimm, D. and Kleinschmidt, J. A. (1999) Progress in adeno-associated virus type 2 vector production: promises and prospects for clinical use. Hum. Gene Ther. 10, 2445–2450. 2. McLaughlin, S. K., Collis, P., Hermonat, P. L., and Muzyczka, N. (1989) Adenoassociated virus general transduction vectors: analysis of proviral structures. J. Virol. 62, 1963–1973. 3. Samulski, R. J., Chang, L. S., and Shenk, T. (1989) Helper-free stocks of recombinant adeno-associated viruses: normal integration does not require viral gene expression. J. Virol. 63, 3822–3828. 4. Clark, K. R., Voulgaropoulou, F., Fraley, D. M., and Johnson, P. R. (1995) Cell lines for the production of recombinant adeno-associated virus. Hum. Gene Ther. 6, 1329–1341. 5. Tamayose, K., Hirai, Y., and Shimada, T. (1996) A new strategy for large-scale preparation of high-titer recombinant adeno-associated virus vectors by using packaging cell lines and sulfonated cellulose column chromatography. Hum. Gene Ther. 7, 507–513. 6. Liu, X. L., Clark, K. R., and Johnson, P.R. (1999) Production of recombinant adeno-associated virus vectors using a packaging cell line and a hybrid recombinant adenovirus. Gene Ther. 6, 293–299. 7. Inoue, N. and Russell, D. W. (1998) Packaging cells based on inducible gene amplification for the production of adeno-associated virus vectors. J. Virol. 72, 7024–7031. 8. Gao, G. P., Qu, G., Faust, L. Z., et al. (1998) High-titer adeno-associated viral vectors from a Rep/Cap cell line and hybrid shuttle virus. Hum. Gene Ther. 9, 2353–2362. 9. Conway, J. E., Rhys, C. M., Zolotukhin, I., et al. (1999) High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap. Gene Ther. 6, 986–993. 10. Clark, K. R., Liu, X., McGrath, J. P., and Johnson, P. R. (1999) Highly purified recombinant adeno-associated virus vectors are biologically active and free of detectable helper and wild-type viruses. Hum. Gene Ther. 10, 1031–1039.


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11. Zolotukhin, S., Byrne, B. J., Mason, E., et al. (1999) Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Ther. 6, 973–985. 12. Grimm, D., Kern, A., Rittner, K., and Kleinschmidt, J. A. (1998) Novel tools for production and purification of recombinant adeno-associated virus vectors. Hum. Gene Ther. 9, 2745–2760. 13. Grimm, D., Kern, A., Pawlita, M., et al. (1999) Titration of AAV-2 particles via a novel capsid ELISA: packaging of genomes can limit production of recombinant AAV-2. Gene Ther. 6, 1322–1330. 14. Yakobson, B., Koch, T., and Winocour, E. (1987) Replication of adeno-associated virus in synchronized cells without the addition of a helper virus. J. Virol. 61, 972–981. 15. Gibson, U. E., Heid, C. A., and Williams, P. M. (1996) A novel method for real time quantitative RT-PCR. Genome Res. 6, 995–1001. 16. Holland, P. M., Abramson, R. D., Watson, R., and Gelfand, D. H. (1991) Detection of specific polymerase chain reaction product by utilizing the 5'-3' exonuclease activity of Thermus aquaticus DNA polymerase. Proc. Natl. Acad. Sci. USA 88, 7276–7280. 17. Clark, K. R., Voulgaropoulou, F., and Johnson, P. R. (1996) A stable cell line carrying adenovirus inducible rep and cap genes allows for infectivity titration of adeno-associated virus vectors. Gene Ther. 3, 1124–1132.

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30 High-Titer Stocks of Adeno-Associated Virus from Replicating Amplicons and Herpes Vectors Ajay R. Mistry, Mahesh De Alwis, Elisabeth Feudner, Robin R. Ali, and Adrian J. Thrasher 1. Introduction The adeno-associated virus (AAV) is a nonpathogenic member of the Parvoviridae family (for review, see ref. 1) Recently this virus has gained considerable interest and has been developed as a gene delivery vector (2). Six primate AAV serotypes (designated AAV types 1–6) have so far been identified and characterized in the literature (3,4). The most extensively studied of these isolates is AAV type 2. The vast majority of the transduction studies have been carried out using recombinant vectors (rAAV) based on serotype 2. These studies have shown that rAAV2 has the ability to transduce a wide range of both dividing and nondividing cells, achieving efficient long-term gene expression in vivo in a variety of tissues including retina (5), muscle (6), central nervous system (7), and liver (8). The range of tissues transduced by recombinant AAV vectors based on other serotypes is currently being investigated by several laboratories (9). It is hoped that rAAV vectors produced from these serotypes may prove to be useful for the transduction of tissues that are poorly infected by AAV2. A major problem associated with the use of rAAV has been the difficulty in producing large quantities of high-titer stock (10,11). This has become an important issue as vectors based on rAAV2 have now reached the stage at which they are starting to be used in human clinical trials (12). This chapter describes the use of the herpes simplex virus type 1 (HSV-1) amplicons that have been developed in our laboratory to attain high-titer stocks of rAAV2 (13). A brief description of the background and basis of the system is given in the first section. From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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1.1. AAV Genome Structure and Organization AAV2 has a single-stranded DNA genome that is 4675 nt long (14). The genome is flanked by inverted terminal repeat sequences (ITRs) that are each 145 nt. The first 125 nucleotides of this sequence are palindromic, which allows it to fold back into a hairpin-like structure. The ITRs are required for AAV2 DNA replication (1) and also contain the sequences necessary to package viral DNA into particles (15). The genome contains two large open reading frames with a single polyadenylation signal. The open reading frame in the 5' half of the AAV genome encodes four nonstructural regulatory proteins (Rep 78, Rep 68, Rep 57, and Rep 40), which have overlapping amino acid sequences; the open reading frame in the 3' half encodes three structural proteins (Vp1, Vp2, and Vp3) in which the amino acid sequences also overlap. The open reading frames are transcribed by three promoters (p5, p19, and p40). The p5 promoter intiates production of a transcript that unspliced encodes Rep 78 and spliced, encodes Rep 68. The p19 is also involved in the transcription of the Rep proteins; it initiates the production of a transcript that is either translated intact to produce Rep 52 or spliced to yield Rep 40. The p40 promoter is involved in the transcription of the genes encoding the AAV structural proteins (Vp1, Vp2, and Vp3). It produces two transcripts by alternative splicing that are at different levels. Vp1 is translated from the minor species, and Vp2 and Vp3 are translated from the major species from different start codons within the same transcript. 1.2. AAV Life Cycle and Conventional Production of rAAV AAV2 belongs to the Dependovirus genus of the Paroviridae family, so-called because it usually requires a helper virus coinfection to allow productive AAV infection to occur. The helper viruses required for this productive lytic process include the adenovirus and HSV. In the absence of helper virus, AAV infects human cell lines and establishes latency as a provirus by integrating into the genome with a high preference for a specific site on human chromosome 19q13.1 (16–18). If the cells containing the AAV provirus are subsequently infected with helper virus, the integrated AAV can be rescued from the chromosome and can enter the productive lytic process (19). Vectors that are deleted for Rep lose the potential for site-preferential integration. Elucidation of the molecular mechanisms involved in the life cycle of AAV is important for its development as a gene therapy vector, especially in terms of recombinant AAV production. The requirement of a helper virus for productive infection of AAV adds to the complexity of the process and has made it more difficult to understand the mechanisms involved. Nevertheless, several systems have been developed to package and produce rAAV. The conventional


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rAAV production system relies on transient transfection of permissive cells and utilizes three components: 1. A plasmid containing the rAAV vector genome. It contains two ITR sequences that flank the cDNA encoding the exogenous gene. The ITR sequences are the minimal cis elements necessary for replication and packaging of the recombinant gene (20). The gene is present within an expression cassette. This is essentially a promoter located before the beginning of the gene that will drive its transcription and a polyadenylation signal at the 3' end of the gene that will stabilize the mRNA transcripts produced. The size of this expression cassette should be between 3.5 and 4.7 kb. 2. A helper plasmid containing the AAV2 genome encoding the rep and cap genes. The four Rep proteins and three Cap proteins are expressed from this plasmid and provide the components in trans required for the assembly of rAAV. 3. Wild-type adenovirus type 5, which provides other helper functions required for the lytic cycle.

The two plasmids are transfected into an appropriate cell line such as 293 or HeLa cells (21,22), and these cells are subsequently infected with the helper adenovirus. This results in the production of infectious rAAV containing the recombinant exogenous gene as the single-stranded vector genome. The rAAV particles can be separated from contaminating adenoviral particles by density gradient centrifugation. However, the inefficiency of this process results in low levels of rAAV virus production, as well as residual contamination with adenoviral components (protein and infectious virus) that may be the cause of inflammatory processes observed in vivo (23). More recently, improvements in transfection efficiency, development of optimized packaging plasmids, and the production of cell lines that stably maintain rep-cap genes have simplified and improved recovery of recombinant virus (10,11,24). In addition, the minimal adenovirus components necessary for helper function are now known, and genes encoding these factors have been cloned into a single plasmid (25,26). This plasmid can be cotransfected along with the helper and ITR plasmids and eliminates the need to carry out the helper virus infection step in the process of making rAAV, thereby eliminating the chance of adenovirus contamination. 1.3. Improving the rAAV Production Systems Although the technical improvements outlined above have achieved some success in raising rAAV titers, none of these systems can achieve the levels of virus that can be produced during a wild-type AAV infectious lytic cycle. Investigations have been carried out to identify the mechanisms that may limit the levels of rAAV production (27). The main findings from these studies showed that during a wild-type infection the numbers of transcriptionally func-

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tional templates available for expression of the Rep78/68, Rep52/40, and capsid gene products are amplified as the whole genome is replicated. During the production of rAAV, the helper plasmid containing the rep-cap genes was found not to replicate after transfection. Thus the lower titer of rAAV particles was thought to be caused by insufficient expression of the Rep and Cap viral proteins. Two types of strategies have been applied in an attempt to overcome this problem. The first strategy is based on the substitution of natural AAV promoters with alternative heterologous elements that increase the transcription levels of the rep and cap genes, resulting in higher levels of Rep and Cap proteins (24,28,29). Increased synthesis of AAV capsid proteins has been shown to improve yields of rAAV (29). However, this approach has not proved satisfactory, as overexpression of Rep gene products has also been shown to decrease rAAV DNA replication and to downregulate expression of the cap genes (24,29). These results indicate that the control and regulation of the rep and cap gene transcription processes by the endogenous promoters (p5, p19, and p40), which allow coordinated production of Rep and Cap proteins, is an important aspect for rAAV production. The second strategy is the use of replicating plasmids that contain sequences encoding the rep and cap genes. The basis of the system is that the plasmid, once transfected into the cell line, will replicate, resulting in an increase in the numbers of rep and cap genomic cassettes and thus overcoming the problem of low rep-cap gene levels. Transcription of the rep and cap genes is still under the control of the endogenous promoters, therefore allowing coordinated production of the Rep and Cap proteins. The system we use to achieve the replication processes is the HSV-1 amplicon plasmids in conjunction with HSV-1 as the helper virus. In contrast to the use of helper adenovirus, replication of these amplicon plasmids containing the rep and cap genomic cassettes, along with HSV-1 as the helper virus, did not markedly inhibit the expression of the Rep proteins (13). These amplicons are considered in more detail below. 1.4. HSV Amplicons HSV-1 has generated substantial interest as a vector to deliver genes to the nervous system because of its natural tropism for neuronal cells. There are two types of HSV-1-based vectors: 1) those produced by inserting the exogenous gene into a backbone virus genome, which are known as recombinant HSV vectors; and 2) HSV amplicon virions, which are produced by inserting the exogenous gene into an amplicon plasmid that is subsequently replicated and then packaged into virion particles (using HSV-1 as a helper virus). These HSV-1 amplicon virions were first described as contaminating defective genomes composed of multiple repetitions of a partial HSV-1 sequence orga-


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Fig. 1. Schematic representation of the use of replicating amplicons to produce rAAV. (A) A helper plasmid containing the AAV2 rep and cap genes and an rAAV plasmid containing transgene flanked by AAV2 ITRs have been cloned into separate amplicon vectors. These vectors each contain an HSV-1 packaging (pac) and an origin or replication (oriS) signals. The two plasmids are transfected into an appropriate cell line. They are then infected with HSV-1 helper virus. (B) This allows replication of the amplicon plasmid that results in the expression of Rep and Cap proteins and the packaging of the transgene to produce rAAV2. (C) In addition to the rAAV2, this process also produces HSV-1 helper virus and HSV-1 amplicon virions, which contain packaged rep-cap sequence and rAAV genome (D).

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nized in a head-to-tail fashion (concatemers). The monomers were shown to consistently include at least one origin of viral DNA replication (oriS) and a DNA cleavage/packaging sequence (pac). Cloning of these two elements in bacterial plasmids was shown to be sufficient to direct concatemeric packaging of the plasmid sequence into HSV-1 amplicon virions in the presence of complementing packaging functions (helper) provided by HSV-1. 1.5. Use of HSV Amplicons to Produce rAAV To exploit the HSV amplicon system for the production of rAAV, the AAV genome containing the rep and cap genes is cloned into an amplicon plasmid. The DNA encoding the rAAV vector genome, i.e., exogenous gene within an expression cassette flanked by two ITR sequences, is also cloned into a separate amplicon plasmid. These two plasmids are transfected into an appropriate cell line and then subsequently infected with an HSV-1 helper virus. This allows the amplicons to replicate, resulting in amplification of the DNA encoding the rep and cap genome and the rAAV genome. The Rep and Cap proteins produced are then utilized to package the rAAV genome to produce the rAAV particles. In addition to the rAAV particles, this process also produces HSV-1 helper virus and HSV-1 amplicon virions, which contain the packaged rep-cap sequence and rAAV genome. The rAAV itself has to be purified away from the cellular material, the HSV-1 helper virus, and the HSV amplicon virions. Figure 1 shows a schematic representation of this system, which we use. Researchers have also shown that the HSV-1 amplicons that have packaged rep and cap sequences along with HSV-1 helper functions can themselves be used to produce rAAV. These amplicons were used to infect a cell line that had been transfected with a rAAV plasmid vector to produce rAAV particles (30). In addition, HSV-1 itself has been engineered to express the AAV2 rep and cap genes. This recombinant HSV-1 was shown to be sufficient in providing the HSV-1 helper functions and the rep-cap sequence in trans for the production of rAAV2 from a cell line that had an integrated AAV2 provirus (31). Attempts have also been made to produce HSV-1 amplicon/AAV hybrid constructs (32). These constructs were essentially amplicon vectors that containing a transgene flanked by AAV2 ITRs along with the AAV2 rep genes under the control of their own endogenous promoters. The transgene in this amplicon was shown to be packaged into rAAV by using the amplicon to infect an appropriate cell line in the presence of an AAV helper plasmid and helper virus. 1.6. Use of DISC-HSV-1 as the Helper Virus Production of the HSV-1 and HSV-1 amplicons in addition to the rAAV may be considered a safety hazard. Although the scheme devised to purify the


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rAAV away from the contaminating HSV-1 and HSV-1 amplicon should be sufficient in terms of safety for most applications, concern may still be raised about the presence of these contaminants, especially if the rAAV is to be used for clinical applications or in large animal models. For these reasons the HSV1 helper virus used in our production system is DISC-HSV-1 (disabled infectious single-cycle virus). This is a genetically deleted herpesvirus that lacks the gene for essential glycoprotein H (gH) but can be propagated to very high titer as an infectious virus in cells expressing gH in trans. In permissive noncomplementing cell lines (gH–), the virus replicates effectively but is noninfective when released. 2. Materials 2.1. Cell Culture 1. Baby hamster kidney cells (BHK). These cells are split 1/6 every 2–3 days. They should not be allowed to overgrow and should be of low passage. The BHK cells can be obtained from European Collection of Animal Cell Cultures (ECACC, cat. no. 85011423). Production of rAAV2 using the BHK cells and the DISCHSV-1 helper should ideally be carried out in BHK cell lines that have a deletion in glycoprotein H (gH–) for the reasons explained in Subheading 1.6. However, BHK cell lines that are not gH– can also be used to produce rAAV2 using the system described here. 2. BHK-21 media (Gibco-BRL). To a bottle containing 500 mL of BHK-21 media, add the following under sterile conditions to produce B10 media: a. 5 mL antibiotic-antimycotic (Gibco-BRL). b. 50 mL of fetal calf serum (FCS), heat inactivated at 56°C for 1 h. c. 25 mL Tryptose Phosphate Broth (Gibco-BRL). d. 5 mL L-glutamine (Gibco-BRL). 3. Phosphate-buffered saline (PBS): 1.0% NaCl, 0.025% KCl, 0.14% Na2HPO4, 0.025% KH2PO4 (all w/v), pH 7.2, sterile. 4. Tissue culture dishes (150-mm diameter). 5. 50-mL polystyrene tubes (Falcon): 17 × 100 mm. 6. Trypsin-EDTA solution (Gibco-BRL).

2.2. Recombinant AAV Plasmid Vectors The plasmid vectors used in this system are shown in Figure 2. The rationale behind the use of the helper plasmid pW7-Helper (Fig. 2b), which consists of the AAV2 rep and cap genes cloned into an HSV amplicon plasmid (pW7-Basic), has been described in Subheadings 1.3. and 1.4. The rAAV amplicon vector that contains the foreign gene cassette is produced in two steps. The first step involves placing the foreign gene cassette between two ITRs by subcloning it into the pTRD-Basic vector (Fig. 2c). The expression cassette flanked by the ITRs is then cut out by digestion with the PacI restriction

Fig. 2. Plasmid vectors used for the generation of rAAV using the HSV amplicon system. (a) pW7-Basic is the amplicon backbone plasmid containing the cis-acting sequences from HSV-1; the pac sequence in which the HSV-1 packaging sequence is located together with the oriS (origin of viral DNA replication). These sequences are required for amplicon genome amplication and packaging during copassage with helper virus. (b) The pW7-Helper plasmid contains the amplicon oriS and pac sequences along with the rep and cap genes. It provides the rep and cap regions of the AAV in trans for the production of rAAV. (c) the pTRD-Basic plasmid contains two ITRs separated by multiple cloning sites. This allows the cloning of the foreign transgene cassette between the ITRs. The construct subsequently produced can be digested with the restriction enzyme PacI (not to be confused with the packaging signal), and the transgene flanked by ITRs excised can be subcloned into the pW7-Basic amplicon plasmid at its PacI site.

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enzyme and then subcloned into the amplicon plasmid vector pW7-Basic, which has a PacI restriction site (Fig. 2a). The plasmids used for transfections are prepared by purification on an ionexhange resin column (e.g., Quiagen Maxi purification kit). 2.3. Generation of Recombinant Virus 1. 2. 3. 4.

Monolayer of BHK cells at approximately 80% confluency. Opti-MEM medium (Gibco-BRL). Lipofectin reagent (Gibco-BRL). Cyclized integrin targeting peptide 6 (KKKKKKKKKKKKKKKKGACRRET AWACG) at 0.1 mg/mL made up in Opti-MEM media. This peptide can be custom ordered from most peptide manufacturers. We obtain ours from Zinsser Analytic (Maidenhead, UK). 5. DNA samples (recombinant AAV plasmid vector and helper plasmid), columnpurified (see Notes 1–3). 6. HSV-1 helper virus: DISC-HSV-1 (see Subheading 1.6.).

2.5. Isolation and Purification of Recombinant Virus 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12.

TMN Buffer: 50 mM Tris-HCl, pH 8.0, 5 mM MgCl2, and 0.15 M NaCl. Benzonase (Merck). 60% iodixanol solution OptiPrep (Sigma). 2 M NaCl solution. PBS MK buffer: 1× PBS, 1 mM MgCl2, and 2.5 mM KCl. Phenol red (0.5% stock solution). Ultracentrifuge tube, 25 × 89 mm (Beckman). Peristaltic pump (e.g., Pharmacia model P1). 10-mL syringe and needle (0.6 × 30 mm). 2.5 mL prepacked heparin-agarose column (Sigma). Elution buffer (PBS MK + 1 M NaCl). Protein concentrators with a molecular weight cutoff of 10,000 Daltons (Amicon Centricon filter devices). 13. Storage buffer: 20 mM Tris-HCl, pH 8.0, 0.15 M NaCl, and 2 mM MgCl2.

3. Methods 3.1. Generation of Recombinant Virus This section describes the methods for transfecting BHK cells with the twoamplicon plasmid followed by infection with helper HSV to produce rAAV particles. The transfection efficiency is critical to the yield of rAAV obtained. We found that the most efficient system to use to transfect BHK cells was the three-component Lipofectin/integrin targeting peptide/DNA (LID) system (33). We routinely produce rAAV from ten 150-mm plates containing BHK cells during a single prep. The transfection procedure described below is for a single

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150-mm dish containing BHK cells. This procedure has to be repeated a further 9 times so that 10 plates in total are transfected. This is important since the procedures described in subsequent sections on the purification of rAAV are based on the use of cells harvested from 10 transfected 150-mm dishes. 3.1.1

. Transfection of DNA Using LID Reagent

The day before transfection 1. Plate out 4.5 × 106 of BHK cells into a 150-mm round tissue culture dish in a total volume of 20 mL. 2. Repeat this procedure for a further nine plates.

The following day: The procedures described below are for a single 150-mm plate containing BHK cells; they must be repeated so that 10 plates in total are transfected (see Note 4). 1. We routinely transfect a total of 60 μg of DNA into a 150-mm dish (see Note 5). For vectors cloned into amplicons, the ratio of the two vectors is 1 (recombinant AAV plasmid vector):3 (rep/cap helper plasmid). Therefore, when using 60 μg of DNA, the amounts of plasmids used are as follows: 15 μg (recombinant AAV plasmid vector):45 μg (helper plasmid). 2. Place the appropriate amounts of each vector into a polystyrene tube to give a final total of 60 μg of DNA. Add 6 mL of Opti-MEM to this tube. 3. Into a separate polystyrene tube place 45 μL (1 mg/mL) of Lipofectin and then add 6 mL of Opti-MEM to it. 4. Add 2.4 mL (at a concentration of 0.1 mg/mL) of the integrin targeting peptide to the tube containing the Lipofectin and mix together by inverting the tube several times (see Note 6). 5. Add the DNA to the polystyrene tube containing the Lipofectin and peptide. Mix by inverting the tube several times. Incubate the tube at room temperature for 1 h to allow time for the complexes to form. 6. Aspirate the medium from the cells and wash the monolayer twice with OptiMEM medium. 7. Add the LID mixture to the cells. 8. Incubate at 37°C under normal 5% CO2 conditions for 5 h. 9. Aspirate the media and replace with B10 media containing HSV-1 at 10–20 IU/ cell. 10. Continue incubation for 32–35 h (see Note 7).

3.2. Isolation and Purification of Recombinant Virus The isolation and purification of the recombinant AAV from the infected BHK cells can be divided into four stages:


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Stage 1. Release of rAAV particles from within the infected BHK cells. Stage 2. Purification of rAAV away from the vast majority of contaminating cellular and viral material by use of a discontinuous iodixanol gradient. Stage 3. Further purification of the rAAV by heparin affinity chromatography. Stage 4. Concentration and dialysis of the rAAV by using protein centrifugal concentrators. 3.2.1. Stage 1: Release of rAAV Particles from within the Infected BHK Cells This stage of the process involves harvesting the infected cells by low-speed centrifugation, resuspension in the hypotonic TMN buffer, lysing the cells by three cycles of freeze thawing, and finally treating the cell lysate obtained with Benzonase to degrade the genomic DNA. 1. Scrape the infected cells and media from the 10 plates into five 50-mL polystyrene tubes. 2. Collect the cells by low-speed centrifugation (250g for 10 min). 3. Resuspend the cell pellets from the 10 plates in a total volume of 15 mL of TMN buffer. At this stage the cells can be stored at –70°C until needed. 4. Carry out three cycles of freeze-thawing in dry ice/ethanol and a 37°C water bath. The cells should be mixed by vortexing in between the cycles. 5. Add 50 U of Benzonase per 1 mL lysate from the 10 plates and incubate at 37°C for 30 min. 6. Clarify the lysate by centrifugation at 2700g for 20 min and retain the viruscontaining supernatant.

3.2.2. Stage 2: Iodixanol Density Gradient Use of the discontinuous iodixanol gradient as an alternative to the CsCl gradient centrifugation has considerably shortened the centrifugation period and in our hands has led to increases in the final titer of purified rAAV. This section describes in detail the procedures we use to make the discontinuous iodixanol gradient and load the clarified lysates onto it. It has mainly been based on the work of Zolotukhin and colleagues (34). 1. In polystyrene tubes make up the following iodixanol solutions by adding the appropriate volumes of solutions, indicated in Table 1: 20 mL of 15% iodixanol 24 mL of 25% iodixanol 15 mL of 40% iodxianol 10 mL of 60% iodixanol 2. Pipet all the cleared lysate (approximately 15 mL) into the bottom of a 25 × 89mm ultracentrifuge tube. Avoid creating air bubbles. 3. Connect the inlet tube from the peristaltic pump to the 15% iodixanol solution

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Table 1 Volumes Required to Make Up Solutions for Discontinuous Iodixanol Gradient 15% 60% Iodixanol stock 10× PBS MK 2 M NaCl Phenol red (0.5 % stock ) ddH2O Final volume

4. 5.

6.

8. 9.

10.

5 2 10 — 3 20

Iodixanol (mL) 25% 40% 10 2.4 — 525 μL 11.1 24

10 1.5 — — 3.5 15

60% 10 — — 30 μL — 10

and pump a small volume of the 15% iodixanol into the tubes to ensure that the dead volume contains this solution. Place the outlet tube from pump into the lysate and allow 9 mL of this solution to enter the centrifuge tube slowly (see Note 8). Remove the inlet tube from the 15% iodixanol solution and place it into the 25% solution. Place the outlet tube into the bottom of the centrifuge tube and allow 6 mL of this solution to enter the centrifuge tube. Repeat this procedure first with the 40% iodixanol solution, allowing 5 mL to enter the centrifuge tube, and then with the 60% solution, allowing enough solution to enter so that the tube is filled to the top (5–6 mL). A discontinuous gradient is formed (see Fig. 3a and Note 9). Seal the tube and place in a ultracentrifuge for 1 h, spinning at 250,000g (without brake) at 18°C. Carefully remove the tube from the centrifuge and place in a clamp stand. The rAAV is located in the 40% iodixanol solution. This 40% band is located between the 60% solution and the 25% solution boundaries, which are marked by the phenol red (Fig. 3b). Insert a needle (0.6 × 30 mm) at the top of the tube to allow air to enter the tube. Using a 10-mL syringe with a needle, carefully insert the needle at the boundary between the 60% iodixanol solution and the 40% solution. Carefully draw out 5 mL of the 40% solution. Add 6 mL of PBS-MK to this eluted 40% iodixanol solution. Put this solution through a 0.1-μm filter (25-mm diameter). This will remove any contaminating particles larger than 0.1 μm such as HSV-1 helper.

3.2.3. Stage 3: Further Purification of rAAV Particles Using a Heparin Column 1. Remove the existing column buffer from a 2.5-mL prepacked heparin-agarose column by spinning the column in a 50-mL polystyrene tube at 15g for 5 min. 2. Equilibrate the column by adding 5 mL of 1× PBS-MK and then spinning at 15g for 5 min. Repeat this procedure 3 more times so that a total volume of 20 mL of PBS-MK has passed through the column.


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Fig. 3. (a) Iodixanol step gradient for the purification of rAAv. The volumes given above are for the 25 ¥ 89-mm ultracentrifuge tubes. The lysate is first pipeted into the bottom of the tube. Nine milliliters of the 15% iodixanol is then pumped into the bottom of the tube. This is followed by pumping 6 mL of the 25% iodixanol, then the 40% iodixanol, and finally 5–6 mL of 60% iodixanol solution to top up the tube. The tube is then sealed and subjected to centrifugation at 58,200 rpm (250,000 g) for 1 h at 18°C. (b) After the 1 h spin, the rAAV is ready to be retrieved from the 40% iodixanol solution. The red or yellow tinge in the 60% and the 25% steps is caused by the phenol red and will help locate the 40% step. The virus is collected by first puncturing a top region of the tube with a needle and then puncturing just below the 40% step with a needle and drawing out approximately 5 mL from this region using a syringe. 3. Add 10 mL of the filtered virus solution to the column, and allowing it to enter by gravity flow. 4. Wash the column by allowing 10 mL of PBS-MK to flow through the column. 5. Elute the virus by adding 6 mL of PBS-MK/1 M NaCl solution. The first 2 mL of the elution can be discarded (dead volume).

3.2.4. Stage 4: Concentration and Dialysis of the rAAV by Using Protein Centrifugal Concentrators The final stage of the process is to concentrate the virus and exchange the solution the virus is in for a more physiologic one (storage buffer). To do this, we simply spin the virus in a centrifugal filter device with a molecular weight cutoff of 10,000 Daltons and then resuspend the virus in 2 mL of storage buffer. The virus is then spun again in the filter device, which is adequate to remove the vast majority of the elution buffer. 1. Place the eluted virus in 2 Centricon filter devices (2 mL each). Spin at 5000g for 50 min at 4°C.

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2. Discard the elution and add 2 mL of storage buffer to each centricon device. Spin again at 5000g for 50 min. 3. Pool the concentrated virus (approximately 150 μL) and store at –70°C.

4. Notes 1. The AAV terminal repeats may be unstable in plasmids propagated in several commonly used laboratory strains of E. coli. Host strains carrying recA, as well as recJ and recB mutations, such as SURE strain cells (Stratagene), are recommended. 2. To ensure that the ITRs in the plasmid that are used for transfections are functional and not deleted, we routinely check the DNA by digesting the plasmid with the restriction enzyme SmaI. The SmaI sites are located within the ITRs; therefore digestion with the SmaI enzyme will cut out the foreign gene expression cassette, indicating that the ITRs are likely to be functional. 3. Use only high-quality DNA for transfections. Either CsCl-banded DNA or DNA prepared using high-grade commercial kits is adequate. 4. The amounts of peptide and Lipofectin used here have been optimized for BHK cells; they may need changing if different cell lines are used. 5. The 1:3 ratios of the two plasmid vectors have been determined systematically in our laboratory. This AAV production system can also be utilized to produce virus from recombinant AAV DNA that is not cloned into an amplicon backbone (albeit with lower titers). We have found that when using such a plasmid the best titers are obtained by using a ratio of 1 (recombinant AAV plasmid vector):1 (helper plasmid). 6. The order in which the LID components are made up are critical for the efficiency of transfection achieved. It is therefore important to mix the peptide and lipid first and then add this mixture to the DNA. 7. During this incubation period the cells are monitored as they undergo the cytopathic process (24–36 h). The cells are harvested just as they start lifting from the plate. 8. The volume that has been pumped into the centrifuge tube can be monitored simply by determining the flow rate of the pump and then allowing the appropriate volume to enter the tube within a timed period. 9. When making up the discontinuous gradient, ensure that the outlet tube from the pump is always at the bottom of the ultracentrifuge tube while the solution is entering the tube.

References 1. Berns, K. I. (1995) Parvoviridae: the viruses and their replication, in Fundamental Virology, 3rd ed. (Fields, B. N., Knipe, D. M., and Howley, P. M., eds.), Lippincott-Raven, Philadelphia. 2. Kotin, R. M. (1994) Prospects for the use of adeno-associated virus as a vector for human gene therapy. Hum. Gene Ther. 5, 793–801. 3. Bantel-Schaal, U. and zur Hausen, H. (1984) Characterization of the DNA of a defective human parvovirus isolated from a genital site. Virology 134, 52–63.


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4. Blacklow, N. R., Hoggan, M. D., Kapikian, A. Z., Austin, J. B., and Rowe, W. P. (1968) Epidemiology of adenovirus-associated virus infection in a nursery population. Am. J. Epidemiol. 88, 368–378. 5. Ali, R. R., Reichel, M. B., Thrasher, A. J., et al. (1996) Gene transfer into the mouse retina mediated by an adeno-associated viral vector. Hum. Mol. Genet. 5, 591–594. 6. Kessler, P. D., Podsakoff, G. M., Chen, X., et al. (1996) Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic protein. Proc. Natl. Acad. Sci. USA 93, 14082–14087. 7. McCown, T. J., Xiao, X., Li, J., Breese, G. R., and Samulski, R. J. (1996) Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector. Brain Res. 713, 99–107. 8. Koeberl, D. D., Alexander, I. E., Halbert, C. L., Russell, D. W., and Miller, A. D. (1997) Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors. Proc. Natl. Acad. Sci. USA 94, 1426–1431. 9. Rutledge, E. A., Halbert, C. L., and Russell, D. W. (1998) Infectious clones and vectors derived from adeno-associated virus (AAV) serotypes other than AAV type 2. J. Virol. 72, 309–319. 10. Clark, K. R., Voulgaropoulou, F., Fraley, D. M., and Johnson, P. R. (1995) Cell lines for the production of recombinant adeno-associated virus. Hum. Gene Ther. 6, 1329–41. 11. Clark, K. R., Voulgaropoulou, F., and Johnson, P. R. (1996) A stable cell line carrying adenovirus-inducible rep and cap genes allows for infectivity titration of adeno-associated virus vectors. Gene Ther. 3, 1124–1132. 12. Kay, M. A., Manno, C. S., Ragni, M. V., et al. (2000) Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector. Nat. Genet. 24, 257–261. 13. Zhang, X., De Alwis, M., Hart, S. L., et al. (1999) High-titer recombinant adenoassociated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H. Hum. Gene Ther. 10, 2527–2537. 14. Srivastava, A., Lusby, E. W., and Berns, K. I. (1983) Nucleotide sequence and organization of the adeno-associated virus 2 genome. J. Virol. 45, 555–564. 15. McLaughlin, S. K., Collis, P., Hermonat, P. L., and Muzyczka, N. (1988) Adenoassociated virus general transduction vectors: analysis of proviral structures. J. Virol. 62, 1963–1973. 16. Kotin, R. M., Linden, R. M., and Berns, K. I. (1992) Characterization of a preferred site on human chromosome 19q for integration of adeno-associated virus DNA by non-homologous recombination. EMBO J. 11, 5071–5078. 17. Kotin, R. M., Siniscalco, M., Samulski, R. J., et al. (1990) Site-specific integration by adeno-associated virus. Proc. Natl. Acad Sci. USA 87, 2211–2215. 18. Samulski, R. J., Zhu, X., Xiao, X., et al. (1992) Targeted integration of adenoassociated virus (AAV) into human chromosome 19 [published erratum appears in EMBO J. 1992; 11, 1228]. EMBO J. 1991; 10, 3941–3950.

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19. Berns, K. I. and Linden, R. M. (1995) The cryptic life style of adeno-associated virus. Bioessays 17, 237–245. 20. Xiao, X., Xiao, W., Li, J., and Samulski, R. J. (1997) A novel 165-base-pair terminal repeat sequence is the sole cis requirement for the adeno-associated virus life cycle. J. Virol. 71, 941–948. 21. Hermonat, P. L. and Muzyczka, N. (1984) Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells. Proc. Natl. Acad. Sci. USA 81, 6466–6470. 22. Samulski, R. J., Chang, L. S., and Shenk, T. (1987) A recombinant plasmid from which an infectious adeno-associated virus genome can be excised in vitro and its use to study viral replication. J. Virol. 61, 3096–3101. 23. Monahan, P. E., Samulski, R. J., Tazelaar, J., et al. (1998) Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophilia. Gene Ther. 5, 40–49. 24. Li, J., Samulski, R. J., and Xiao, X. (1997) Role for highly regulated rep gene expression in adeno-associated virus vector production. J. Virol. 71, 5236–5243. 25. Xiao, X., Li, J., and Samulski, R. J. (1998) Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus. J. Virol. 72, 2224–2232. 26. Matsushita, T., Elliger, S., Elliger, C., et al. (1998) Adeno-associated virus vectors can be efficiently produced without helper virus. Gene Ther. 5, 938–945. 27. Fan, P. D. and Dong, J. Y. (1997) Replication of rep-cap genes is essential for the high-efficiency production of recombinant AAV. Hum. Gene Ther. 8, 87–98. 28. Flotte, T. R., Barraza-Ortiz, X., Solow, R., et al. (1995) An improved system for packaging recombinant adeno-associated virus vectors capable of in vivo transduction. Gene Ther. 2, 29–37. 29. Vincent, K. A., Piraino, S. T., and Wadsworth, S. C. (1997) Analysis of recombinant adeno-associated virus packaging and requirements for rep and cap gene products. J. Virol. 71, 1897–1905. 30. Conway, J. E., Zolotukhin, S., Muzyczka, N., Hayward, G. S., and Byrne, B. J. (1997) Recombinant adeno-associated virus type 2 replication and packaging is entirely supported by a herpes simplex virus type 1 amplicon expressing Rep and Cap. J. Virol. 71, 8780–8789. 31. Conway, J. E., Rhys, C. M., Zolotukhin, I., et al. (1999) High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap. Gene Ther. 6, 986–993. 32. Johnston, K. M., Jacoby, D., Pechan, P. A., et al. (1997) HSV/AAV hybrid amplicon vectors extend transgene expression in human glioma cells. Hum. Gene Ther. 8, 359–370. 33. Hart, S. L., Arancibia-Carcamo, C. V., Wolfert, M. A., et al. (1998) Lipid-mediated enhancement of transfection by a nonviral integrin-targeting vector. Hum. Gene Ther. 9, 575–85. 34. Zolotukhin, S., Byrne, B. J., Mason, E., et al. (1999) Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Ther. 6, 973–985.

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31 Herpes Simplex Virus/Adeno-Associated Virus Hybrid Vectors for Gene Transfer to Neurons Preparation and Use Lauren C. Costantini, Cornel Fraefel, Xandra O. Breakefield, and Ole Isacson

1. Introduction Gene transfer to the central nervous system (CNS) has shown major advances in recent years, with the development of novel vector systems and progress in basic virology (1–12). To improve gene transfer to CNS neurons, we have combined the critical elements of herpes simplex virus-1 (HSV-I) amplicons and recombinant adeno-associated virus (AAV) vectors to construct a hybrid amplicon vector, and then packaged the vector into HSV-1 virions via a helper virus-free system. These HSV/AAV hybrid amplicon vectors have shown efficient transduction and stability of transgene expression in neurons (and other nondividing cell types [13]), both in culture and after intracerebral injection with no apparent toxicity or immune response, as well as extended transgene expression in dividing cells (14). Before detailing the hybrid amplicon vectors, a short description of the two vectors upon which the hybrid amplicon vectors are based is given.

1.1. Characteristics of HSV-1 and AAV One of the most comprehensively studied viruses for gene transfer is HSV-1. The approximately 300-nm enveloped virus contains an icosahedral capsid encasing 152 kb of double-stranded DNA encoding over 80 genes, 38 of which are dispensable for virus replication in culture (15). The virion shows high infectivity for neurons and glia, as well as many other cell types (16), and From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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enters the cell by fusion of the envelope with the plasma membrane. The capsid is transported along microtubules to the nucleus, where the viral DNA circularizes and then replicates, enters latency, or is degraded. Two types of vectors are derived from HSV-1: recombinant virus vectors and amplicon vectors (for review, see ref. 17), the latter of which is utilized in the hybrid amplicon vectors. The HSV-1 amplicon plasmid bears an HSV-1 origin of DNA replication, oris, and a DNA cleavage/packaging signal, pac. ori allows the amplicon to be replicated by a rolling-circle mechanism, producing long concatenates of DNA that are subsequently cut into unit-length HSV1 genomes at pac during packaging into capsids in the presence of HSV-1 helper functions (18,19). Amplicon DNA is thereby packaged into HSV-1 virion, and after infection of cells, the amplicon concatenate assumes an extrachromosomal state in the infected cell nucleus. When packaged free of helper virus, these amplicon vectors show essentially no toxicity or antigenicity, as they express no virus genes. Since the combined size of oris and pac is 35 kb) (2). In addition, the natural biology of HSV-1 infection involves long-term persistence of the viral genome in a latent, nonintegrated state in neuronal cell nuclei (3–5) and other postmitotic cell types in the absence of viral protein synthesis, genome integration, or interference From: Methods in Molecular Medicine, Vol. 69, Gene Therapy Protocols, 2nd Ed. Edited by: J. R. Morgan © Humana Press Inc., Totowa, NJ

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Fig. 1. HSV-1 virion structure and genome organization. (A) Schematic illustration of the HSV virion, showing the capsid, tegument, and glycoprotein-containing lipid envelope. (B) Schematic representation of the HSV genome, showing the unique long (UL) and unique short (US) segments, each bounded by inverted repeat (IR) elements. The locations of the essential genes, which are required for viral replication in vitro, and the nonessential or accessory genes, which may be deleted without affecting replication in vitro, are indicated. The IE gene and other important gene loci are in capitals.

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with host cell biology. Since the virus does not disrupt normal host cell biology or express viral antigens during latency, cells harboring latent virus will not be attacked by the host’s immune system and should allow persistence of the viral genome for the lifetime of the host, obviating the need for repeat dosing of the virus vector. During latency the viral genome is transcriptionally silent except for expression of a set of viral latency-associated transcripts (LATs) (6–11). Since the LATs are not required for establishment or maintenance of this latent state (12–18), it should be possible to delete these genes and replace them with the desired therapeutic gene to drive expression of this gene product from an otherwise quiescent genome using the latency and neuronal cell-specific promoter complex resident within the vector genome. 1.1. The HSV-1 Life Cycle The HSV-1 particle (Fig. 1A) is composed of 1) an envelope containing 10 glycoproteins that allow the virus to attach to and infect cells by fusion of the virus envelope with the cell surface membrane (for review, see ref. 19–21); 2) a tegument matrix inside the envelope composed of viral structural components involved in shutoff of host protein synthesis (22–25), activation of immediate early viral gene expression, and assembly functions (26–31); 3) a regular icosahedral-shaped nucleocapsid (32); and 4) a linear double-stranded DNA genome containing approximately 85 open reading frames (33–36). The 152-kb viral genome is segmented (Fig. 1B), with each of its long (UL) and short (US) unique segments flanked by inverted repeats (IRs). The viral functions have been categorized as to whether they are essential for virus replication in cell culture or are accessory (nonessential) functions that contribute to virus replication and spread in vivo. The viral genes are arranged in such a manner that many of the essential functions or accessory genes tend to be clustered within the genome. Additionally, since very few HSV-1 genes are spliced and the virus possesses a highly evolved recombination system, it is relatively easy to manipulate and engineer HSV-1 for purposes of gene transfer by deleting individual genes or blocks of genes that may play a role in vector toxicity. During normal infection, HSV-1 infects the skin following direct contact and undergoes a productive (lytic) infection in skin fibroblasts and epithelial cells (Fig. 2A). The initial binding of virus to the host cell involves the interaction of glycoproteins B and C (gB and gC) with cell surface heparan sulfate moieties (37–39). This is followed by the binding of gD to specific cell surface receptors HveA (40–45) and HveC (45–49), which are members of the tumor necrosis factor-α/nerve growth factor (TNF-α/NGF) receptor superfamily and the immunoglobulin superfamily, respectively. Binding of gD to HveA/HveC initiates the fusion event between the host cell surface membrane and the viral envelope (50–53), a process that also requires the functions of gB (54) and the

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Fig. 2. HSV-1 life cycle. (A) Schematic diagram of the HSV-1 lytic replication cycle in vivo. HSV-1 binds to and enters mucosal or epithelial cells and proceeds through the lytic replication pathway. Following uncoating, the virion is transported to the nucleus, where the linear viral genome is injected through a nuclear pore. The lytic cascade of viral gene expression ensues, with subsequent replication of the viral genome. The resulting progeny virus particles can encounter and fuse with the cell surface membrane of peripheral nerve termini, which innervate the site of primary infection. The viral nucleocapsid then travels via retrograde axonal transport to the neuronal cell body, where the virus can either proceed through the highly regulated cascade of lytic gene expression, or enter latency, during which the viral lytic gene program is interrupted and the latency-associated transcripts (LATs) are the sole viral RNAs expressed. In response to a wide variety of stimuli, the virus is capable of reactivating from the latent state, entering the lytic portion of the HSV life cycle, at which time progeny virions can either be transported back to the site of the primary infection or the virus may enter the central nervous system. (B) Temporal cascade of HSV-1 gene expression detailing the roles of HSV-1 immediate early (IE) gene transactivators ICP4, ICP27, ICP22, and ICP0 and the IE promoter stimulatory molecule VP16. The IE (or α) genes are expressed immediately upon infection in the absence of de novo protein synthesis. The VP16 (αTIF, Vmw65) virus tegument protein interacts with the cellular factor Oct-1 to regulate expression of the IE genes positively by binding to their promoters. The IE gene products ICP4, ICP27, and ICP0 are responsible for activating early (E or β) genes. Following viral DNA replication, the ICP4, ICP22, and ICP27 IE polypeptides regulate the expression of the late (L or γ) genes.


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gH/gL complex (55–57). Following uncoating of the particle, cellular molecular motors transport the viral nucleocapsid to the nuclear membrane, where the viral linear dsDNA genome is injected through a pore into the host cell nucleus. Once within the nucleus, the lytic replication cycle of the virus takes place (58,59), with the viral genes expressed in a highly regulated cascade (60,61) of coordinated gene expression consisting of three stages: immediate early (IE or α), early (E or β), and late (L or γ) (Fig. 2B). Three of the viral IE genes are transcriptional activators that induce expression of E and L genes (62–69). Early gene functions participate in viral DNA replication, which must proceed in order for late gene expression to occur (70,71). The late genes encode largely structural products comprising the nucleocapsid, tegument, and viral envelope glycoproteins. Viral particles are assembled within the nucleus and bud from the nuclear membrane; particle maturation proceeds during migration through the Golgi apparatus, followed by egress from the cell. Following focal replication of the virus in these permissive cell types, the virus invades the nervous system by directly infecting axon terminals of local sensory neurons of the peripheral nervous system (PNS) (72,73). The viral nucleocapsids are transported in a retrograde manner back to the neuronal cell body, where the virus can either replicate or enter latency. During latency the linear viral genome circularizes, becomes methylated, and forms a higher order nucleosomal structure (3–5,74). At this point the lytic genes become inactive and the LATs are readily detected by in situ hybridization using LAT-specific riboprobes (8– 11,17). The virus can remain within the latent state for the lifetime of the individual, or it can be induced to reactivate from latency by a variety of stimuli, resulting in the resumption of the lytic cycle and the subsequent synthesis of progeny virions, which may traverse the axon by anterograde transport, establishing an active infection at or near the site of primary infection. 1.2. Engineering HSV-1 Vectors The optimal HSV vector should be 1) safe and completely devoid of replication-competent virus; 2) noncytotoxic; 3) incapable of affecting normal host cell biology; 4) able to persist in the neuronal cell body in a nonintegrated state; and 5) capable of expressing the therapeutic gene(s) to appropriate levels at the proper time(s). The three major considerations in the design of HSV-1 vectors concern the elimination of the cytotoxic properties of the virus, the ability to target binding and entry of the virus to the specific cells or tissues of interest, and the development of promoter systems for proper expression of the therapeutic gene. Considerable effort has been expended in addressing these issues of vector design. In this work we will concentrate on the engineering of HSV-1 vectors deleted for essential gene functions that display reduced toxicity following infection.

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1.2.1. Solving the Problem of HSV-1 Cytotoxicity Since UV-irradiated virus displays substantially reduced cytotoxicity in vitro (75,76) and disruption of viral IE gene expression by interferon also reduces toxicity, it is presumed that the cytotoxicity of HSV-based vectors results from the expression of HSV-1 gene products. The fundamental approach to designing HSV-1 vectors with reduced toxicity is to remove the essential IE genes (Fig. 1B) of the virus, as well as several nonessential genes whose products interfere with host cell metabolism and are part of the virion (tegument) structure. Deletion of the two essential IE genes that encode the infected cell proteins 4 (ICP4) and 27 (ICP27) blocks early and late gene expression (62,77,78) (Fig. 2B). These deletions require that the missing functions be supplied in trans, using a complementing cell line (62,77,79) to propagate virus. To ensure that recombination does not occur between the defective virus and the viral sequences present within the complementing cell line during propagation, it is essential that these sequences not share homology with sequences present within the viral genome and that the deletion of the IE genes from the virus exceed the limits of the complementing sequences. Since many of these viral IE genes are toxic to cells, expression of the complementing genes must be inducible upon infection with the defective virus. This is achieved through the use of HSV-1 IE promoters to drive expression of these toxic transactivating genes from the cell, since these promoters have been shown to respond to the HSV-1 transactivator VP16 (Vmw65 or α-TIF) (27–31), a virion tegument component that accompanies the viral DNA molecule into the nucleus of the infected cell. VP16 recognizes a consensus sequence (octomer-TAATGARAT) located at various sites in all HSV-1 IE promoters; together with the cellular transcription factors octomer binding protein one (Oct-1) and HCF (also termed C1, VCAF-1, and CFF) (80–84), VP16 transactivates the IE gene promoters (85–89). In the absence of virus infection, the complementing IE genes in the cell chromosome are silent. However, upon infection with the replication-defective mutant, the VP16/Oct-1/HCF complex transactivates the IE promoters upstream of the complementing viral sequences in the cell line, thereby inducing expression of the necessary products for propagation of the deletion virus. A third IE gene of interest is ICP0, which is both cytotoxic and capable of promiscuous transactivation of a variety of cellular genes (64,90–92); it also enhances the level of expression of other viral genes (90). ICP0 appears to collaborate cooperatively with ICP4, for example, to increase the activity of this key viral function (93,94), although ICP0 is not a promoter binding protein and thus appears to stimulate an event prior to direct promoter activation (95). Although ICP0 is a nonessential viral function, deletion of ICP0 results in decreased viral titers (67,96), and propagation of high-titer stocks of virus


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deleted for ICP0 in conjunction with the essential IE genes will require the production of a cell line capable of complementing ICP0 as well as ICP4 and ICP27. Generation of such a line has been extremely difficult, since even lowlevel synthesis of ICP0 is toxic to the host cell (97). The two remaining IE genes, ICP22 (which affects the phosphorylation of RNA polymerase II) (98) and ICP47 (which affects the processing of MHC class I antigens) (99-101), may also need to be deleted depending on the specific therapeutic application. In addition to the viral IE gene functions, an additional gene remains a target of interest for removal to reduce toxicity. The infecting virus carries in with the particle a tegument component that has a virion-associated host shutoff (vhs) activity (22,23). vhs appears to interfere nondiscriminately with mRNA stability (24). Removal of the UL41 (vhs) gene does not affect viral replication (25) but enhances the health of the cell upon infection with nonreplicating viral mutants (102). Deletion of a combination of the four IE regulatory genes (ICP4, ICP22, ICP27, and ICP0) along with UL41 (vhs) has yielded vectors that display diminished toxicity for a variety of cell types in culture (103–106). Recombinants deleted for both ICP4 and ICP27 (103–106) were less toxic than the ICP4/ ICP27 single IE gene deleted viruses d120 (77) or 5dl1.2 (107). The removal of three of the IE gene (ICP4, ICP22, and ICP27) dramatically reduced cytotoxicity (103,106) and led to increased duration of vector-mediated transgene expression in neurons in culture (103). Recombinants that failed to express any of the five IE genes including ICP0 essentially shut down viral gene expression upon infection of noncomplementing cells, rendering the virus safe and noncytotoxic (105). However, transgene expression from these recombinants was transient or undetectable in many cell types (105), owing to deletion of the ICP0 gene (97,105). Thus, it may prove necessary to retain ICP0 to achieve expression of the therapeutic gene product. For some specific therapeutic applications, the retention of expression of ICP47, which has recently been shown to downregulate MHC class I antigen expression (99–101), should provide an additional level of protection from immune surveillance at the initiation of infection in vivo. 1.2.2. Construction of Mutant Viruses Deleted for IE and Other Toxic Functions The first generation of replication-defective mutant viruses consisted of mutants deleted for the essential ICP4 gene. One of these recombinants, designated d120, can be grown on a complementing cell line (E5) that expresses ICP4 in trans upon infection with the ICP4 deletion mutant virus (77). We have subsequently introduced the β-galactosidase (lacZ) reporter gene, under control of the strong human cytomegalovirus (HCMV) immediate early gene

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promoter into the thymidine kinase gene locus of the genome of this replication-defective mutant, in order to identify rapidly cells and tissues infected with this vector to evaluate the potential uses of such vectors. We have shown that the transgene was transiently expressed in a variety of cell types in culture and in various tissues in vivo (108,109). Long-term expression of the transgene both in culture and in some cells in vivo may be affected by the virus-induced toxicity, leading to death of the cells in culture and/or immune recognition and clearance in vivo. Therefore, it was clear that additional IE genes must be removed to reduce viral toxicity further. To generate second-generation replication-defective viruses deleted for multiple IE essential gene functions, it was necessary to construct a cell line to complement the essential IE gene functions. A cell line was constructed to complement both ICP4 and ICP27 by transfecting Vero cells with a plasmid containing the HSV-1 sequences coding for ICP4 and ICP27 along with a neomycin expression (SV2-neo) cassette for rapid selection of individual clones. To eliminate the chance of homologous recombination and rescue of the mutant viruses during propagation in the complementing line, the plasmid containing the coding regions for ICP4 and ICP27 was engineered to avoid overlap of these sequences with the deletions present within the virus. One clone, designated 7b, was isolated after multiple rounds of drug selection; this clone was able to complement the growth of the IE deletion mutants d120 (ICP4-) (77) and 5dl1.2 (ICP27-) (107). A second-generation double-mutant virus deleted for both ICP4 and ICP22 was engineered using the 7b cell line (Fig. 3). This recombinant, DHZ.1, was engineered by recombining the linearized plasmid pB5, containing the HCMV IE promoter-lacZ BGHpA cassette surrounded by ICP22 flanking sequences, into the ICP22 gene locus of the ICP4 replication-defective mutant d120. Positive recombinants were propagated and isolated on the 7b complementing cell line owing to the production of blue plaques following X-gal staining. The DHZ.1 recombinant fails to replicate or produce the blue plaque phenotype on normal noncomplementing (Vero) cells. To engineer a third-generation triple IE gene-deleted vector, we simply crossed DHZ.1 (ICP4-/ICP22-) with the ICP27 mutant 5dl1.2 (107). Recombinants deleted for the three IE genes (Fig. 3) were selected for the production of blue plaques on the 7b double IE complementing cell line compared with viruses that would only plaque on either the ICP4-expressing line (E5) or the ICP27-expressing line (N23). The triple IE gene-deleted vector THZ.1 was employed in a genetic cross with the UL41 gene mutant ΔSma (110) to engineer a vector deleted for ICP4, ICP27, and ICP22 and the vhs gene product (Fig. 3). The structure of each recombinant vector was confirmed by Southern blot analysis.


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Fig. 3. Construction of multiply deleted HSV vectors. The construction of multiple gene deletion mutants can be accomplished by either standard homologous recombination or by genetic cross. The ICP4-/ICP22- double IE gene deletion mutant (DHZ.1) was constructed by cotransfection of d120 (77) viral DNA with the plasmid pB5 (in which ICP22 sequences were replaced with an HCMV IEp-lacZ BGHpA cassette) in the 7b (ICP4/ICP27) complementing cell line. The desired ICP4-/ICP22recombinants were identified by the production of a blue plaque phenotype on 7b cells following X-gal staining, and their genome structure was confirmed by Southern blot analysis. The triple IE gene deletion mutant THZ.1 was produced by crossing DHZ.1 with the single ICP27 deletion mutant 5dl1.2 (107). Progeny viruses that were lacZ positive and replicated on 7b (ICP4/ICP27) cells but not E5 (ICP4) or N23 (ICP27) cells were selected and confirmed by Southern blot analysis. The mutant THZ.3 was engineered by crossing THZ.1 with the UL41 mutant ΔSma (25).

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The DHZ.1 double mutant and other double mutants deleted for different combinations of IE genes were examined for reduced toxicity in cell culture compared with both the first-generation single IE gene-deleted (ICP4-) parental virus and the third-generation vectors deleted for three IE genes (THZ.1 and THZ.3). In this particular study, Vero cells were infected with the various viruses at a multiplicity of infection (MOI) of 1.0, and the number of viable cells was determined at 24 h post infection using trypan blue exclusion. In addition, we determined the number of apoptotic cells in culture using the FragEL (Roche, Indianapolis, IN) DNA fragmentation kit. This specific MOI was chosen since d120 uniformly kills cells at an MOI of 1 or greater. As shown in Table 1, the double DHZ.1 mutant is less cytotoxic than the SHZ.1 single IE gene mutant for Vero cells at an MOI of 1.0, although some toxicity still remains. Double IE gene deletion mutants lacking ICP22 and either ICP4 (DHZ.1) or ICP27 (DHZ.3) were less toxic than the ICP4/ICP27 (DHZ.4) double gene mutant. In addition, removal of three IE toxic genes (THZ.1) as well as other toxic gene targets such as vhs (THZ.3) further reduced HSV vector toxicity to the point that it eventually approached that observed with mockinfected cells (Table 1). We have obtained similar results with these recombinant vectors both in various cell types in culture and in vivo (103). The cassette that was recombined into the ICP22 locus is unique in that it contains the lacZ gene construct flanked by two 8-bp recognition sites for restriction endonuclease PacI that are not present at any other site in the viral genome. Thus, the expression cassette can be easily removed by digestion with the PacI restriction enzyme followed by religation of the genome, yielding a recombinant with a single PacI site that produces clear plaques on the 7b complementing cell line (111). To introduce a new gene cassette efficiently into the ICP22 locus of this recombinant, the recombinant genome is cleaved with PacI and used in marker transfer transfection assays with plasmid-containing sequences that span the PacI site in ICP22 (111). The desired recombinant will lack the HCMV-lacZ expression cassette and thus can be easily isolated as a clear plaque on a background of blue plaques produced by the parental virus. The recombination frequency obtained using this approach is 10-fold greater than that seen in standard marker rescue experiments (111) since the background generated by the parental viruses is greatly reduced owing to digestion of the parental viral DNA with PacI. We have employed this method to generate a number of recombinants including a vector THD (Fig. 4) that expresses the full-length dystrophin gene product for gene therapy applications to treat Duchenne muscular dystrophy (1).


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Table 1 Cytotoxicity of Recombinant HSV Vectorsa Vector Mock SHZ.1(ICP4-) DHZ.1(ICP4-/ICP22–) DHZ.3(ICP22-/ICP27-) DHZ.4(ICP4–/ICP27–) THZ.1(ICP4–/ICP22–/ICP27–) THZ.3(ICP4–/ICP22–/ICP27–/UL41–)

% Survival

% Apoptotic

100 52 80 85 75 >100 >100

0.3 15.6 3.6 2.5 6.2 0.6 0.1

aVero cells were either mock-infected or infected with the single IE gene mutant SHZ.1 (ICP4-

), the double IE gene deletion mutants (DHZ.1, DHZ.3, and DHZ.4), or the triple IE gene (ICP4/ICP22-/ICP27-) deletion mutants (THZ.1 and THZ.3) at an MOI = 1.0. The numbers of viable cells were counted at 1 day post infection by trypan blue exclusion. The number of cells in the culture undergoing apoptosis was determined using the FragEL detection kit (Roche). Subsequent deletion of the additional cytotoxic IE gene led to increased cell survival and a decrease in Vero cell apoptosis compared with the single IE gene deletion virus (SHZ.1). Deletion of ICP22 from the ICP4 backbone had the greatest effect on vector-induced toxicity. Deletion of UL41 from the triple IE gene-deleted virus backbone (THZ.3) only marginally affected toxicity.

2. Materials 1. Vero (African green monkey kidney, ATCC, cat. no. CCL81) cells. Other permissive cells such as HELs or BHKs, or complementing cell lines are required to propagate HSV-1 accessory or essential gene deletion viruses. 2. MEM/10% FCS: Eagle’s modified essential medium (MEM) supplemented with nonessential amino acids, 100 U/mL penicillin G, 100 μg/mL streptomycin sulfate, 2 mM glutamine, and 10% fetal calf serum (FCS). 3. TBS, pH 7.5: 50 mM Tris-HCl, pH7.5, 150 mM NaCl, 1 mM EDTA. 4. Lysis buffer: 10 mM Tris-HCl, pH 8.0, 10 mM EDTA. 5. TE: 10 mM Tris-HCl, pH 8.0, 1 mM EDTA. 6. TE equilibrated phenol/chloroform/isoamyl alcohol (25:24:1 v/v). 7. 2× HBS: 20 mM HEPES, 135 mM NaCl, 5 mM KCl, 5.5 mM dextrose, 0.7 mM Na2HPO4, pH 7.05. Accurate pH of this solution is critical. 8. X-gal staining solution that contains the chromogenic substrate X-gal at a final concentration of 300 μg/mL in TBS containing 14 mM K4Fe(CN)6, 14 mM K 3Fe(CN) 6. X-gal is highly insoluble and must be dissolved in dimethyl formamide (DMF) prior to addition to the staining solution. 9. 1.0% methylcellulose overlay: Add 25 g methylcellulose to 100 mL phosphatebuffered saline (PBS), pH 7.5, in a 500-mL sterile bottle containing a stir bar. Autoclave the bottle on the liquids cycle for 45 min. After the solution cools, add 350 mL of MEM supplemented with nonessential amino acids, 100 U/mL penicillin G, 100 μg/mL streptomycin sulfate, and 2 mM glutamine. Mix well and

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Fig. 4. Use of the PacI method to generate a replication-defective HSV vector expressing the full-length dystrophin cDNA (DMD). The 14-kb dystrophin cDNA was cloned downstream from the HCMV IE promoter in the ICP22 shuttle plasmid that contains adequate HSV flanking DNA sequence, to allow efficient homologous recombination at the ICP22 gene locus of the vector. The expression cassette can then be introduced into the ICP22 locus of the THZ.1 vector by PacI digestion of THZ.1 viral DNA and the subsequent cotransfection of the PacI-digested THZ.1 DNA along with the shuttle plasmid containing the DMD expression cassette. (A) THZ.1 contains a lacZ expression cassette at the ICP22 locus of a vector deleted for ICP4, ICP27, and ICP22 and produces blue plaques following X-gal staining. (B) The new recombinant, THD, can be isolated following homologous recombination of the shuttle plasmid into the PacI-digested THZ.1 genome by the identification of clear plaques. Following three rounds of limiting dilution analysis, the structure of THD can then be confirmed by Southern blot analysis (1). place the bottle on a stir plate at 4°C overnight. Once the methylcellulose has entered solution, add 50 mL of FCS. 10. 1× PBS, pH 7.5: 135 mM NaCl, 2.5 mM KCl, 1.5 mM KH2PO4, 8.0 mM Na2HPO4, pH 7.5.

3. Methods 3.1. Isolation of Viral DNA for Transfection To engineer a new virus recombinant, plasmid is required containing the particular sequence of interest flanked by sufficient amounts of viral sequences


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homologous to the desired gene locus within the HSV-1 genome along with purified, infectious viral DNA. The quality and purity of these two reagents will determine the frequency of generating the desired recombinant virus. It is imperative that the sequence of interest in the transfer plasmid contain at least 500–1000 bp of flanking HSV-1 sequences to achieve a higher frequency of producing and isolating the recombinant. The quality of the viral DNA used in the transfections to synthesize new recombinants can be evaluated by two criteria: 1) whether the DNA is intact and at the proper concentration, as determined by Southern blot analysis (112); or, more importantly, 2) whether the viral DNA is infectious and capable of producing an optimal number of plaques following transfection of 1 μg of viral DNA. We have optimized the protocol for the production of highly infectious viral DNA and routinely obtain preps in which 1 μg of purified viral DNA will yield 100–1000 plaques (see Note 1). 1. Infect a subconfluent to confluent monolayer of cells in a T150 tissue culture flask at an MOI of 3. The cell should have been split at both 1 and 3 days prior to infection. 2. Allow the infection to proceed for approximately 18–24 h depending on both the cell type and virus used. All cells should be rounded–up and still adherent to the flask, yet just about ready to detach. 3. Remove the cells by tapping the flask or use a cell scraper to dislodge the cells. 4. Pellet the cells for 5–10 m at 2060g at 4°C in a 15-mL conical polypropylene tube. 5. Wash the cells 1× with 10 mL of TBS (pH 7.5). 6. Lyse the cells in 5 mL of lysis buffer (10 mM Tris-HCl, pH 8.0, 10 mM EDTA) + 0.25 mg/mL Proteinase K + 0.6% sodium dodecyl sulfate (SDS). 7. Wrap the lid of the tube in parafilm and incubate the tube on a nutator platform at 37°C overnight. 8. Extract the suspension 2× with phenol/chloroform/isoamyl alcohol (25:24:1), being careful not to be too vigorous. However, it is important to invert the tube enough to achieve proper mixing of the phases. When removing the aqueous phase, remember to leave the interface behind, as the DNA stays at this point, thus increasing the overall yield. 9. Extract the aqueous phase 2× with chloroform, again being careful during mixing. 10. Remove the aqueous phase to a new tube, going as close to the interface as possible. The DNA present at the interface is extremely viscous and will enter the pipet as a visible slurry. 11. Add 2 vol of cold isopropanol to precipitate. Mix well. 12. The DNA can be spooled on a heat-sealed Pasteur pipet, or the mixture can be stored at –20°C overnight. If spooling the DNA, remove the spooled DNA and transfer the pipet to a new tube, breaking off the Pasteur pipet. Let dry overnight and then resuspend in 0.5–1.0 mL TE buffer or dH20 using wide-bore pipet tips (see Note 2).

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At this point, it is important to determine the quality of the DNA prep (see Note 3). The DNA concentration was determined spectrophotometrically at 260 nm. Southern blot analysis of digests 1 μg quantities of the DNA prep with several diagnostic restriction enzymes should determine whether the DNA is intact. Transfection of 1 μg quantities of the DNA prep into permissive tissue culture cells will allow the determination of the number of infectious particles per 1 μg of DNA. 3.2. Construction of Recombinant Virus: Transfection of Plasmid/Viral DNA Once the proper transfer plasmid has been constructed, by deleting the HSV1 gene of interest yet maintaining sufficient HSV-1 flanking sequences to allow efficient recombination into the viral genome, it is then possible to markertransfer these sequences into the virus, taking advantage of the highly active recombinational machinery of the virus (see Note 4). This is accomplished by transfecting both linearized plasmid and PacI-digested purified viral DNA into permissive cells using the calcium phosphate method (113,114). To readily detect the desired recombinants containing the desired therapeutic gene of interest, the target parental virus backbone should possess a reporter gene cassette (i.e., lacZ or green fluorescent protein [GFP]) at the desired site of recombination. Positive recombinants obtained from the transfection will produce clear plaques compared with the blue plaque phenotype of the parental virus. Alternatively, the introduction of a reporter gene cassette along with the therapeutic gene within the transfer plasmid will allow for more rapid identification and purification of the desired recombinant virus from the ensuing transfection reaction when the parental virus lacks a reporter gene. 1. Split Vero cells (for deletion of nonessential HSV-1 genes) or the specific complementing cell line (for deletion of essential HSV-1 gene[s]) 1:10 3 days prior to transfection. 2. At 1 day prior to transfecting, split the cells again and plate in 60-mm tissue culture dishes at a cell density of 1 × 106 cells/plate in MEM/10% FCS. 3. Linearize the plasmid construct at a restriction enzyme site between the flanking HSV-1 sequence and any E. coli DNA present within the bacterial vector (see Note 3). 4. Digest the purified viral DNA with PacI to completion. 5. Make up the transfection mixture by adding 1–5 μg from the viral DNA prep (the amount of DNA that yields 200 or more plaques by transfection) to an amount of linearized plasmid DNA (or restriction fragment) equal to 10× and 50× genome equivalents of viral DNA. Viral DNA or plasmid DNA alone are used as controls for the transfection (see Note 5).


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6. Add 600 μL of 2× HBS to each tube, mix, and place on ice for 20 min (see Note 6). 7. Add 41 μL of 2 M CaCl2 dropwise, mixing gently. Set at room temperature for 20 min (see Note 7). 8. Aspirate the media from the plates and rinse 1x with 1 mL of 2× HBS. 9. Pipet transfection mixture up and down to break up large clumps of precipitate, add carefully to cell monolayers, and place plates at 37°C for 40 min in a CO2 incubator. 10. Add 4 mL MEM/10% FCS per plate and place at 37°C for 4 h in a CO2 incubator. 11. Aspirate media from plates and wash 1× with 1 mL of HBS, being careful not to cause the cell monolayer to lift off the plate. 12. Slowly and carefully add 2 mL of 20% glycerol (dilute 100% glycerol in 2× HBS) per plate and leave on cells at room temperature for exactly 4 min (see Note 8). 13. Carefully remove all of the glycerol shock solution by aspiration and wash the monolayer 3× with 2 mL of MEM/10% FCS. Be sure the monolayer remains intact. 14. Carefully add 4 mL of MEM/10% FCS and incubate the plates at 37°C in a CO2 incubator. 15. Observe the plates twice daily under the microscope for the production of complete cytopathic effect (CPE), indicating the presence of infectious foci. This usually takes 3–5 days depending on the virus and cell type used to propagate the recombinant. 16. Once a majority of the cells have rounded up, remove the media and store it temporarily at 4°C. Isolate the virus from the cell pellet by three cycles of freezethawing and sonication followed by centrifugation at 913g for 5 min at 4°C. Then combine this supernate with the removed media and store at –80°C for use as a stock.

This stock of virus can now be analyzed for the presence of recombinants and purified as described in the next section. 3.3. Isolation and Purification of Recombinant Virus The stock of virus obtained from the transfection can now be used to isolate the desired recombinant. It is necessary to isolate and purify the recombinant through three rounds of limiting dilution. This process can be greatly enhanced by the inclusion of a reporter gene cassette within the sequences to be recombined back into the viral genome or by the disruption of a reporter gene cassette following homologous recombination of the therapeutic gene cassette into the parental virus genome that already possesses the reporter cassette. We have optimized the limiting dilution procedure for the detection of recombinants expressing the β-galactosidase (lacZ) reporter gene.

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3.3.1. Limiting Dilution Procedure for the Detection of Recombinants Expressing LacZ The advantage of employing limiting dilution is that it does not require the standard plaque isolation technique in which single, well-isolated plaques are picked following agarose or methylcellulose overlay. Contamination of positive recombinants with parental virus represents a considerable problem using the standard plaque isolation procedure since it is difficult to find well-isolated plaques on a plate, or virus from an adjacent plaque gets sucked up along with that from the designated plaque in the act of picking a plaque through the agarose or methylcellulose overlay. 1. Titer the stock of recombinant virus from the transfection. 2. Add 30 plaque-forming units (pfu) of virus to 3 mL of 1 × 106 cells in suspension (MEM/10% FCS) within a 15-mL conical polypropylene tube. 3. Wrap the lid of the tube with parafilm, and place the tube on a nutator rocker platform at 37°C for 1 h. 4. Following the 1-h period for virus adsorption, add 7 mL of fresh media, and plate 100 μL of the mixture in each well of a 96-well flat bottomed plate. 5. Incubate the plates at 37°C in a CO2 incubator for 2–5 days until the appearance of plaques. 6. The plates are scored for wells containing only single plaques. Theoretically, by adding 30 pfu, it should be possible to obtain 30 of 96 wells that contain single plaques. 7. Transfer the media from each well into a new 96-well plate. Store the plate at –80°C for future use as a virus stock. 8. Stain each well of the plate by adding 100 μL of the X-gal staining solution using a multichannel pipetor (see Note 9). 9. Incubate the plates at 37°C in a CO2 incubator overnight or for several hours until the appearance of readily detectable blue plaques.

Wells containing single blue or clear plaques are scored and the overall frequency of original recombination event is determined. Media from the frozen stock 96-well plate stored at –80°C can now be used in the next round of the limiting dilution procedure. With each subsequent round of limiting dilution, the ratio of desired recombinants within the population should approach 100%. We will routinely proceed through one additional round of limiting dilution after the ratio reaches 100% to ensure purity of the stock. At this point, the virus stock can be used to produce a midi-stock for the eventual preparation of a high-titer stock for general experimental use. At the same time, this stock is used to produce viral DNA to confirm the presence of the insert as well as the absence of the deleted sequences by Southern blot analysis (112) (see Note 10).


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3.4. Preparation of High-Titer Stocks of Recombinant Virus Prepare a midi-stock of recombinant virus from a monolayer of cells in a T25 tissue culture flask and obtain the titer of the stock for preparation of the final stock. 3.4.1. Titration of Virus Stock This procedure can be used to obtain the titer of any size virus stock. 1. Seed 6-well tissue culture plates with 0.5–1.0 × 106 cells per well at 1 day prior to titration of the stock. 2. Prepare a series of 10-fold dilutions (10-2 to 10-10) of the virus stock in 1 mL of cold MEM without serum. 3. Add 100 μL of each dilution to a near confluent monolayer of cells in a single well of a 6-well tissue culture plate (in duplicate). 4. Allow the virus to adsorb for a period of 1 h at 37°C in a CO2 incubator. Rock the plates every 15 min to distribute the inoculum. 5. Aspirate off the virus inoculum, add 3 mL of 1.0% methycellulose overlay, and reincubate the plates for 3–5 days, until well-defined plaques appear. 6. Aspirate off the methycellulose, and stain with 1 mL of 1% crystal violet solution (in 50:50 methanol/dH2O, v/v) for 5 min. The stain fixes the cells and virus. Alternatively, the wells can be stained using the X-gal solution if the virus contains a lacZ reporter cassette. 7. Aspirate off the stain, rinse gently with tap water to remove excess stain, and airdry. 8. Count the number of plaques per well, determine the average for each dilution, and multiply by a factor of 10 to get the number of pfu/mL for each dilution. Multiply this number by 10 to the power of the dilution to achieve the titer in pfu/ mL.

3.4.2. Virus Stock Preparation The following procedure calls for preparing a virus stock from two roller bottles worth of cells; however, it can be scaled up or down depending on specific needs (see Note 11). 1. We routinely infect 5–10 roller bottles of cells with virus to produce a high-titer stock. Each roller bottle is infected with virus at an MOI of 0.01–0.05, depending on the particular vector backbone, in a volume of 20 mL of serum-free media (DMEM; Gibco-BRL, Life Technologies) for 2 h. 2. After the 2-h adsorption period, add 80 mL of media (DMEM/10% FCS; GibcoBRL) to each roller bottle. Then observe the bottles by light microscopy to determine the optimal time for harvesting virus. This time has been shown to vary dramatically depending on the particular vector backbone. Generally, viral CPE

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3. 4. 5.

6.

7. 8. 9.

10.

Goins et al. should be obvious, with the majority of the cells rounded up yet not detached from the roller bottle surface. Harvest the cells by scraping the cell monolayer into the media. Collect medium and subject it to low-speed centrifugation at 2060g for 5 min at 4°C. Store the supernatant on ice. Resuspend the cell pellet in a minimal volume (2–5 mL) of serum-free media and subject it to three rounds of sonication to disrupt it and release cell-associated virus. Following low-speed centrifugation (2060g for 5 min at 4°C) to remove the cellular debris, combine this supernatant with the supernatant from the first lowspeed spin. Clarify this preparation further using an additional low-speed spin at 10–17,000g for 5 min. Then pellet the virus by centrifugation at 48,400g in 50-mL Oak Ridge tubes for 30 min at 4°C. Resuspend the virus pellet isolated following a high-speed spin in 500 μL of serum-free media per roller bottle of virus-infected cells and mix with OptiPrep solution (22% OptiPrep, 0.8% NaCl, 10 mM HEPES, 1 mM EDTA). Centrifuge the sealed tubes at 645,000g for 3.5 h in a Beckman Vti65.2 or Vti90 rotor at 4°C. Following the centrifugation period, harvest the virus from the gradient. We routinely detect three bands of varying intensity depending on the particular vector backbone on the gradient. Harvest the lower two bands: approximately 60% of the virus is present in the second band from the bottom of the gradient. Alternatively, fractionate the tubes and determine the titer of each fraction. Then aliquote the vector stocks and store at –80°C until use.

The titer of the stock can be determined by the virus titration procedure detailed above. If concentration is not required, the OptiPrep solution acts as a cryopreservative. However, the virus can be furthered concentrated by centrifugation in a microfuge at 15,115g and 4°C. Following centrifugation, the viral pellet is resuspended in a minimal volume of PBS containing glycerol or dimethyl sulfoxide (DMSO). It is necessary to add glycerol to a final concentration of 10% to the virus stock to cryopreserve the virus properly. 4. Notes 1. The DNA that is produced using the viral DNA isolation technique is not composed exclusively of viral DNA but also contains cellular DNA. The cellular DNA in this mixture acts as carrier when precipitating the DNA during the isolation, thus increasing the yield of DNA. In addition, the cellular DNA acts as carrier DNA during transfections and increases the overall efficiency of forming a precipitate, thereby increasing the chance of obtaining the desired recombinant. If necessary, pure viral DNA can be prepared from virus harvested solely from the


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media of infected cells or from virus particles that have been gradient purified. The yield of DNA obtained in this instance is significantly reduced. The use of wide-bore pipetman tips (Bio-Rad, Hercules, CA) will help prevent shearing of the viral DNA, thereby increasing the infectivity of the viral DNA prep. The quality of the viral DNA preparation is crucial to the recombination frequency. Quality can be evaluated by Southern blot or by determining the number of infectious centers following transfection. We have found that some preparations will appear to be intact by Southern blot analysis, yet still contain a significant number of viral genomes that are nicked and thus are not infectious. It is important that the preparation yield 100–1000 plaques/μg of viral DNA. The quality of the plasmid DNA also plays a role in the recombination frequency. Two to five hundred base pairs of HSV-1 flanking sequence is sufficient; however, ≥1 kb will dramatically increase the chance of isolating the desired recombinant. The size of the sequence to be inserted into the HSV-1 vector genome can affect the generation of the desired recombinant. It is possible for the virus to package up to an additional 10% of the genome, 15 kb for wild-type virus and potentially more for single and multiple gene-deleted viruses. If the insert is too large or contains sequences that affect the stability of the viral genome, part or all of the insert will be lost over time and it will not be possible to obtain a purified isolate of the desired recombinant. The specific gene locus targeted for insertion/ deletion can affect the recombination event. Recombination into the repeat sequences can yield a mixture of viruses containing insertion into one or both copies of the gene. The recombinational machinery of the virus can convert an isolate with a single copy into a recombinant with inserts in both copies. The same mechanism can also produce virus lacking the insert in both copies (i.e., wild-type virus). Southern blot analysis can confirm whether the insert is present in 0, 1, or 2 copies. It is important to linearize the plasmid construct before transfection to increase the recombination frequency compared with that obtained with uncut supercoiled plasmid. Digestion of the plasmid to release the insert, followed by purification of the restriction fragment, does not increase the recombination frequency. Although the frequency is the same, use of purified fragment is superior since no chance exists for the insertion of plasmid vector sequences into the virus by semihomologous recombination. The pH of the HBS transfection buffer (HEPES) is extremely crucial to the transfection efficiency. Depending on the cell type being transfected, other buffers such as BBS (BES) or PiBS (PIPES) may result in higher efficiencies. Other transfection procedures can also be employed that will produce equivalent or greater recombination frequencies. Lipofectamine (Gibco-BRL) can be employed instead of the calcium phosphate method; however, other liposome preparations have not proved effective for the transduction of the large 152-kb HSV genome.

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8. Glycerol or DMSO can be used to shock cells during transfection. The percentage of glycerol or DMSO used depends on the cell type being transfected. We have found that glycerol is less toxic than DMSO for Vero cells and that 20% glycerol produced the highest number of transformants with the lowest level of toxicity. 9. Bluo-gal can be substituted for X-gal in the X-gal staining solution. Although Bluo-gal is more costly than X-gal, it is superior since it produces a darker blue reaction product with reduced background staining of the cell monolayer and it has a greater solubility in DMF. 10. The viral DNA mini-prep procedure routinely yields enough DNA for three to five restriction enzyme digestions for Southern blot analysis. 11. Virus stocks should be maintained at a low passage. Use one vial of a newly prepared stock as a stock for preparing all future stocks. To reduce the chance of rescuing wild-type virus during the propagation of viruses carrying deletions of essential gene(s), stocks should be routinely prepared from single plaque isolates.

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Index AAV, see Adeno-associated virus Acellular dermis, see Skin substitute Adeno-associated virus (AAV), genome structure, 446, 462 herpes simplex virus amplicons for hightiter stock production, amplicon features, 448, 450 cell culture, 451 DISK-HSV-1 as helper virus, 450, 451 materials for production, 451, 453 plasmids, 451, 453, 458 purification of recombinant virus, concentrating, 457, 458 heparin affinity chromatography, 456, 457 iodixanol density gradient, 455, 456, 458 overview, 454, 455 release from infected cells, 455 rationale, 450 transfection, 453, 454, 458 herpes simplex virus-1 hybrid vector for gene transfer to neurons, advantages, 464, 465 components, 465 cosmid DNA preparation for transfection, 467, 470–472, 475, 476 gene transfer, animals, 469, 474–476 neuron culture, 469, 474, 476 helper virus-free stock preparation, 467, 468, 472, 473, 476 materials for production, 465, 467, 468, 475 packaging, 463, 464, 467 plasmid construction, 469, 470 rationale, 461–463

Adeno-associated virus (AAV) (cont.), herpes simplex virus-1 hybrid vector for gene transfer to neurons (cont.), safety, 464, 465 titration, 468, 473, 474 transduction efficiency, 464 protein function, 446 recombinant vector production, DNase-resistant genome quantification, 438, 439, 441, 442 materials, 431–433 midscale production screen, 432, 436, 437, 441 optimization strategies, 447, 448 packaging cell lines, 429–432 plasmids, 447 polymerase chain reaction assay of infectious virus, 439, 440, 442 producer plasmid generation, 431–434, 440 purification, 430, 432, 433, 437, 438, 441 requirements, 427–429, 447 titration, 430, 431, 433, 438–442 transfection, 435, 436, 440 replication, 446 serotypes, 445 transduction efficiency, 427 transgene integration, 462 tropism, 427, 445 Adenovirus, advantages in gene transfer, 371, 389 first generation vectors, overview, 371 genome, 389–391 helper-dependent vector system, cell culture, 377 concentration determination, 384 design of vector, 373, 375

509

510 Adenovirus (cont.), helper-dependent vector system (cont.), helper virus, 375, 376, 385 materials, 373, 375–377 overview, 373 purification of vector, 376, 377, 381, 383, 384, 386 rationale, 371, 372 rescue and amplification, 376–380, 385 restriction enzyme digest analysis, 384–386 Southern blotting for amplification monitoring, 380, 381, 385, 386 ovine vectors, cell culture, 420, 422–424 cell lines for production, 422 design, 416, 417 genome structure, 415, 416 genomic plasmids, 417 materials for production, 417, 418, 420 purification, 423, 424 rationale for construction, 415 recombinant genome generation, direct cloning, 420, 421 recombination in Escherichia coli, 421, 422, 424 shuttle plasmids, 417, 418 titration, 424, 425 protein functions, 390, 391 replication, 391 replication-deficient vectors, 391 serotypes, 389 tumor vaccine modification, 236 two-plasmid rescue system, cell culture, 395, 402, 412 cesium chloride banding of virus, 398, 408, 409 concentration determination, 409 genomic plasmids, 393, 395 materials for production, 393, 395, 397–399 monolayer cell production, 398, 407 optimization of production, 411, 412 overview, 391–393 plasmid preparation, 399, 401, 412

Index Adenovirus (cont.) two-plasmid rescue system (cont.), replication competent virus assay, 410, 411 restriction enzyme digest analysis, 405, 409, 412 shuttle plasmids, 395 suspension cell production, 398, 407, 408 titration, 397, 406, 412 transfection, 395, 397, 402, 404, 405, 412 AFM, see Atomic force microscopy AIPcS2a, see Photochemical transfection Asialoorosomucoid, gene therapy targeting of liver, asialoorosomucoid-lysine methyl esterVSVG peptide conjugate synthesis, 19, 20 asialoorosomucoid-polylysine-listeriolysin O conjugate synthesis, asialoorosomucoid-polylysine conjugation, 18 DNA complex formation, 19 listeriolysin O synthesis and conjugation, 18 cell transfection and luciferase reporter assay, 21, 22 DNA compaction measurement, 21, 27 materials, 16, 17 mouse liver transfection, 22 particle size determination, 21 PEG-polysine conjugate synthesis, PEG-polysine, 20 PEG-polysine-VSV, 20 PEG-polysine-VSV/asialoorosomucoidpolylysine-DNA complexes, 20– 22 rationale, 15, 16, 25 stability of complexes, 21 Atomic force microscopy (AFM), DNA conjugate particle size analysis, 41, 42 B BAM, see Bioartificial muscle Bioartificial muscle (BAM), advantages and disadvantages, 220, 221

Index Bioartificial muscle (BAM) (cont.), applications, 220 formation, cell culture, 222, 228 materials, 221–223 Matrigel seeding and maintenance, 222, 223, 227, 230 primary mouse muscle cell isolation, 221, 223–225, 229 retroviral transduction, 222, 225, 228– 230 silicone tissue mold fabrication, 222, 226 implantation, 223, 227, 228, 230 principles of ex vivo therapy, 219, 220 C Cytokine-modified tumor vaccine, see Tumor vaccine D Di-n-propylsulfoxide (DPSO), solvoplex vectors, 84, 85 synthesis, 89, 90 DNA vaccine, gene gun, see Gene gun muscle, 49, 50, 58, 109 DPSO, see Di-n-propylsulfoxide E Electron microscopy, DNA conjugate particle size analysis, 4 Electroporation, muscle delivery of genes, advantages over viral vectors, 55 applications, 55, 56 duration of expression, 54, 55 efficiency of gene delivery, β−galactosidase, 59, 60 interleukin-5, 59 overview, 49, 50, 59, 110 GeneSwitch system, 115–117, 119 instrumentation, 56, 57 parameters affecting efficiency, DNA concentration, 52 electrical field direction, 53 pulse length and number, 52 voltage of pulses, 51, 52

511 Electroporation, muscle delivery of genes (cont.), technique, 58 vector, 53, 54, 56, 60 F Feline immunodeficiency virus (FIV), gene transfer vectors, advantages, 335 cell culture, 342 concentrating, 343, 345, 348 first generation vectors, 338 harvesting, 343, 345, 348 infection, overview, 345, 346 Retronectin utilization, 346, 349, 349 spinoculation of target cells, 346 supernatant infection, 346 materials for production, 342, 343 plasmids, 342, 343 pseudotyping, 340, 341 second generation vectors, 339–341 third generation vectors, 341 titration, 347, 348 transfection, calcium phosphate, 342–344, 348 FuGENE 6, 342–344, 348 tropism, 341, 342 genome, 337 replication, 337, 338 FIV, see Feline immunodeficiency virus Foamy virus, see Simian foamy virus-1 G Gaucher's disease, gene therapy clinical trials, 189–192 Gene gun, advantages, 137, 144 applications, 137, 144 devices, 138, 139 discharge and transfection, 142 DNA cartridge preparation, 1441 DNA vectors and coating on gold, 139– 141 elemental gold particle preparation, 139

512 Gene gun (cont.), gene expression assays, cytokines, 141, 143 β−galactosidase, 140, 143 hAAT, 140, 143 luciferase, 140, 143 tissue extraction, 142, 143 materials, 139–141 skin preparation, 140, 142 GeneSwitch system, electroporation, 115–117, 119 injection, 115 materials, 114–116 mifepristone induction, 112, 113, 115, 117 nonsecreted gene product assay, 118 plasmids and formulation, 111, 112, 114, 115, 116, 118, 119 principle, 111, 112 promoters, 113, 114 secreted gene product assay, 118–120 Genetically modified skin substitute, see Skin substitute H Hemagglutinating virus of Japan (HVJ), liposome gene transfer, animal studies, 70 artificial viral envelope liposomes, 64–66 cationic lipoids, 65 cultured cell studies, 70 efficiency, 63, 65, 66 preparation of conjugates, DNA complex preparation, 69, 70 flow chart, 68 lipid mixture preparation, 69 materials, 66, 67 virus preparation from eggs, 68, 69 repeated injection, 63, 64 safety, 65 Hematopoietic stem cell (HSC), abundance, 188 CD34+ enrichment, antibody selection, 187 Ceprate system, 195 requirement for gene transfer, 188 expansion ex vivo, 188, 189

Index Hematopoietic stem cell (HSC) (cont.), functional assays, 187, 188 markers, 188 retroviral transduction ex vivo, clinical grade amphotropic vector generation, 193–195, 197 clinical trials, 189–192 materials, 192, 193 multidrug resistance engineering, 190 optimization, 189, 192 prestimulation of cells, 196 transduction, efficiency, 190 protocol, 196, 197 Herpes simplex virus-1 (HSV-1), adeno-associated virus hybrid vector for gene transfer to neurons, advantages, 464, 465 components, 465 cosmid DNA preparation for transfection, 467, 470–472, 475, 476 gene transfer, animals, 469, 474–476 neuron cultre, 469, 474, 476 helper virus-free stock preparation, 467, 468, 472, 473, 476 materials for production, 465, 467, 468, 475 packaging, 463, 464, 467 plasmid construction, 469, 470 rationale, 461–463 safety, 464, 465 titration, 468, 473, 474 transduction efficiency, 464 advantages in gene therapy, 481, 483 amplicons for high-titer adeno-associated virus stock production, amplicon features, 448, 450, 462 cell culture, 451 DISK-HSV-1 as helper virus, 450, 451 materials for production, 451, 453 plasmids, 451, 453, 458 purification of recombinant virus, concentrating, 457, 458 heparin affinity chromatography, 456, 457

Index Herpes simplex virus-1 (HSV-1) (cont.), amplicons for high-titer adeno-associated virus stock production (cont.), purification of recombinant virus (cont.), iodixanol density gradient, 455, 456, 458 overview, 454, 455 release from infected cells, 455 rationale, 450 transfection, 453, 454, 458 genome, 483 protein functions, 483, 485 replication, 461, 462, 483, 485 replication-defective vectors for gene transfer, cytotoxicity of recombinan vectors, 490, 491 DNA isolation for transfection, 492– 494, 498, 499 double mutant virus lacking ICP4 and ICP22, 488, 490 engineering goals, 485 first generation vectors, 487, 488 immediate early gene targeting for cytotoxicity reduction, 486, 487 limiting dilution for β−galactosidase expressing recombinants, 496, 500 materials for production, 491, 492 second generation vectors, 488, 490 stock preparation, 497, 498, 500 titration, 497 transfection, 494, 495, 499, 500 structure, 461 HIV, see Human immunodeficiency virus HSC, see Hematopoietic stem cell HSV-1, see Herpes simplex virus-1 Human immunodeficiency virus (HIV), constitutive transport element in simple retroviruses, 280, 281 function of proteins, Env, 260, 277 Gag, 260, 277 Nef, 260, 277, 279, 280 Pol, 260, 277 Rev, 260, 279, 305

513 Human immunodeficiency virus (HIV) (cont.), function of proteins (cont.), structural proteins, 277 Tat, 260, 278, 279, 304, 305 Vif, 260, 280 Vpr, 260, 277, 280, 305 Vpu, 260, 280 gene transfer vectors, advantages and limitations, 264, 265, 275, 286, 287, 319 applications, 308 cell culture, 265, 266, 270, 289, 293, 309, 310, 315 central DNA flap creation, 285 concentrating, 266, 268, 288, 290, 294, 295, 309, 310, 312, 313, 315 design and performance, 263, 264 first-generation vectors, 284 β−galactosidase reporter gene assay, 310, 313–315 green-fluorescent protein-encoding vector detection, 291, 292, 295 harvesting, 312, 315 materials for production, 265, 266, 287–289, 309–311 p24 assay, 266, 269, 270 plasmids, 265, 266, 270 replication-competent retrovirus assays, 266, 269, 288, 289, 292, 293, 295, 307 Rev-independent vectors, 284 safety in production, 307 self-inactivating vectors, 284, 285, 306 stability, 308 Tat-independent vectors, 284 titration, 266, 269, 270, 288, 290–292, 310, 313–315 toxicity, 308 transfection using calcium phosphate precipitation, 268, 270, 287– 290, 294, 309–311, 315 vesicular stomatitis virus G glycoprotein hybrids, 261, 285, 306, 308, 319

514 Human immunodeficiency virus (HIV) (cont.), gene transfer vectors (cont.), woodchuck hepatitis virus posttranscriptional regulatory element modification, 285 genome, 259–261, 276, 304 packaging cell system, components, 281, 306 plasmids, elimination of Vif, Vpr, and Vpu, 282 first generation plasmids, 281, 282 preparation, 309, 314, 315 pTV, 306 pTY, 306, 307 Rev-independent plasmids, 283 segregation of Gag/Gag-Pol and Rev functions, 282 segregation of Gag and Pol coding regions, 282–283 titer, 307, 308 types, 261, 263, 285, 286 replication, 277, 278, 303–305 structure, 259 HVJ, see Hemagglutinating virus of Japan L, K Keratinocyte, see Skin substitute Lentiviral vectors, see Feline immunodeficiency virus; Human immunodeficiency virus; Simian immunodeficiency virus Light-induced gene delivery, see Photochemical transfection Liposome, liposome-polycation-DNA, see Liposome-polycation-DNA viral liposomes, see Hemagglutinating virus of Japan Liposome-polycation-DNA (LPD), formulations, 73 gene transfer efficiency, 74, 75 preparation, 73 incubation conditions, 76, 77, 80 liposome preparation by thin-film hydration and extrusion, 78–80 materials, 76, 79

Index Liposome-polycation-DNA (LPD) (cont.), size, 74 storage, 74 toxicity, 75 Listeriolysin O, synthesis and asialoorosomucoid-polylysinelisteriolysin O conjugation, 18 Liver, gene therapy targeting with protein delivery systems, asialoorosomucoid-lysine methyl esterVSVG peptide conjugate synthesis, 19, 20 asialoorosomucoid-polylysine-listeriolysin O conjugate synthesis, asialoorosomucoid-polylysine conjugation, 18 DNA complex formation, 19 listeriolysin O synthesis and conjugation, 18 cell transfection and luciferase reporter assay, 21, 22 DNA compaction measurement, 21, 27 materials, 16, 17 mouse liver transfection, 22 particle size determination, 21 PEG-polysine conjugate synthesis, PEG-polysine, 20 PEG-polysine-VSV, 20 PEG-polysine-VSV/ asialoorosomucoid-polylysineDNA complexes, 20–22 rationale, 15, 16, 25 stability of complexes, 21 Low-density lipoprotein receptor, gene delivery mediation, 33 LPD, see Liposome-polycation-DNA Lung, applications of gene delivery, 83 polymeric immunoglobulin receptor, gene delivery mediation, 34 solvoplex gene delivery, advantages, 83, 84 di-n-propylsulfoxide synthesis, 89, 90 formulations and efficiencies, 84, 85 intratracheal injection, mouse, 90–93 rat, 91

Index Lung (cont.), solvoplex gene delivery (cont.), mechanism of transfection, 87 plasmid preparation, 88, 89 preparation, 90, 92 readministration, 87 reporter gene studies, β−galactosidase, 91–93 green fluorescent protein, 92, 93 luciferase, 91, 93 overview, 86 rodents for study, 88, 92 solvents, 88 storage, 86 toxicity, 87 M Mannose receptor, gene delivery mediation, 34 Mifepristone, see GeneSwitch system MMLV, see Moloney murine leukemia virus Moloney murine leukemia virus (MMLV), see Retrovirus Muscle, bioartificial muscle, see Bioartificial muscle DNA vaccine, 49, 50, 58, 109 electroporation, advantages over viral vectors, 55 applications, 55, 56 duration of expression, 54, 55 efficiency of gene delivery, β−galactosidase, 59, 60 interleukin-5, 59 overview, 49, 50, 59, 110 instrumentation, 56, 57 parameters affecting efficiency, DNA concentration, 52 electrical field direction, 53 pulse length and number, 52 voltage of pulses, 51, 52 technique, 58 vector, 53, 54, 56, 60 regulated gene therapy, GeneSwitch system, electroporation, 115–117, 119 injection, 115

515 Muscle (cont.), regulated gene therapy (cont.), GeneSwitch system (cont.), materials, 114–116 mifepristone induction, 112, 113, 115, 117 nonsecreted gene product assay, 118 plasmids and formulation, 111, 112, 114, 115, 116, 118, 119 principle, 111, 112 promoters, 113, 114 secreted gene product assay, 118– 120 ligand-dependent systems, overview, 110, 111 rationale, 110 N Neuron gene transfer, see Herpes simplex virus-1 P PBMC, see Peripheral blood mononuclear cell Peripheral blood mononuclear cell (PBMC), replication-competent retrovirus assay, 292, 293 Photochemical transfection, advantages and limitations, 126, 127 cell culture, 127–129, 132 DNA/poly-L-lysine complex preparation, 128–130, 132 in vivo potential, 127 light sources and dosing, 128, 130–132 materials, 127, 128 photosensitizer, AIPcS2a solution preparation, 129, 132 cytotoxicity and cancer photodynamic therapy, 125, 126 definition, 123, 124 intracellular localization, 124, 125 reactions, 124 structures, 125 principle of photochemical internalization, 123 transfection reaction, 130, 132, 133

516 PLL, see Poly-L-lysine Poly-L-lysine (PLL), binding assay using fluorescence quenching, 9 charge ratio determination, 9 copolymer conjugate synthesis, calculation based on composition, 9 materials, 4, 5 nuclear magnetic resonance, 8 PL26k-graft-(ε−NH-CH2CO-NHPEG−ε−trilactose ligand)2.5, 6, 8 poly-L-lysine-graft-R1-graft-R2-graft-R3, 5, 6 graft, attachment, 3, 4 structure, 2 ligand, 3 luciferase gene expression study, 10, 11 nucleic acid delivery rationale, 1, 2, 15 particle size analysis, 10 PEG-polysine conjugate synthesis for liver targeting, PEG-polysine, 20 PEG-polysine-VSV, 20 PEG-polysine-VSV/ asialoorosomucoid-polylysineDNA complexes, 20–22 photochemical transfection, DNA/poly-Llysine complex preparation, 128–130, 132 plasmid DNA preparation, 8 polyplex formation, 9, 10 Polymeric immunoglobulin receptor, gene delivery mediation, 34 R RDO, see RNA-DNA oligonucleotide hybrid Receptor-mediated gene delivery, see also Asialoorosomucoid; SEC-R, DNA compaction importance, 27, 28 endosomal escape and nuclear uptake, 29, 30 ligands, 26 mechanism, 26, 27 polycations in DNA condensation, 28, 29 rationale, 15, 16, 25

Index Receptor-mediated gene delivery (cont.), receptor types and ligands, asialoglycoprotein receptor, 33 low-density lipoprotein receptor, 33 mannose receptor, 34 polymeric immunoglobulin receptor, 34 SEC-R, 34, 35 table, 31, 32 transferrin receptor, 33, 34 Retrovirus, see also Feline immunodeficiency virus; Human immunodeficiency virus; Simian foamy virus-1; Simian immunodeficiency virus, advantages for gene transfer, 173 alphavirus for cytoplasmic vector construction, see Semliki forest virus, bioartificial muscle gene transfer, see Bioartificial muscle hematopoietic stem cell gene transfer, see Hematopoietic stem cell keratinocyte ex vivo retroviral gene transfer, see Skin substitute titer assays, active virus per cell determination, 165, 169 cell culture, fibroblasts from human foreskin, 167, 168 materials, 166, 167 cell surface area determination by fluorescence microscopy, 167– 169 factors affecting titer, 161, 162 β−galactosidase assay, 167, 168, 171 multiplicity of infection determination, 165 recombinant retrovirus harvesting, 168 serial dilution, 161 start of infection, active virus concentration, 162–164, 169–172 transduction efficiency of different cell types, determination, 165, 166, 170, 171

Index Retrovirus (cont.), transduction efficiency, 149 transgene cassette stability, 173, 174 tumor vaccine, see Tumor vaccine vesicular stomatitis virus G glycoprotein pseudotyping of murine leukemia retrovirus, cell culture, 153 concentrating, 156 env protein replacement, 150 materials, 153, 154 packaging cell, 150, 151 plasmids, 153 producer cell line generation, 155, 156 pseudotransduction, 152 rationale, 149, 150 titration, 156 transduction efficiency, 151, 152, 156, 157 transduction protocol, 154 transfection, 153–155, 157 RNA-DNA oligonucleotide hybrid (RDO), gene conversion, assays, bacterial transformation assay for gene correction in eukaryotic cells, CC106 competent cell preparation, 103, 104 P90C competent cell preparation, 102, 103 principle, 102 transformaton and plating, 104, 105 cell culture, 99 materials, 99, 100, 105 mutant β−galactosidase plasmid reactions, 101, 102, 105 nuclear extract isolation, 99–101, 105 overview, 96, 102 comparison of different cell types, 96–99 point mutation correction, 95 S SEC-R, cell distribution, 35 ligand, 34, 35

517 SEC-R (cont.), receptor-mediated gene delivery, conjugate analysis, 36, 39, 43 conjugate construction, 35–39, 42, 43 DNA condensation, 36, 37, 39–42 DNA plasmid preparation, 36 materials, 35–37, 42 particle size analysis, atomic force microscopy, 41, 42 electron microscopy, 41 overview, 37, 41 Semliki forest virus (SFV), replication, 174 retrovirus cytoplasmic vector construction, analysis of vectors, 182, 183, 185 cell culture, 176, 183, 184 minigene incorporation, 175, 176 packaging cell line, 182, 185 plasmids, 176, 178, 179, 184 principles, 174, 175, 183 RNA synthesis, 178, 179, 181, 184 titration, 178, 184 virus production, 178, 181, 182, 184, 185 Sendai virus (SeV), gene transfer vector, cell culture, 365, 366 F-defective vector design, 362, 363 green fluorescent protein as reporter, 364, 365, 367–369 inducible expression of F protein, 366, 367 infection, 368 materials for production, 365, 366, 368 overview of generation, 363–365 packaging cell line construction, 363 photoinactivation of recombinant vaccinia virus, 366 propagation, 368 titration, 368 genome, 361, 362 liposome generation, see Hemagglutinating virus of Japan protein functions, 362, 363 replication, 361

518 SeV, see Sendai virus SFV, see Semliki forest virus SFV-1, see Simian foamy virus-1 Simian foamy virus-1 (SFV-1), advantages in gene transfer, 319, 320 gene transfer vectors, cell culture, 325 development, 322, 323 infection of nonadherent cells, 326, 328 materials for production, 325, 326 packaging cell lines, 324–326 plasmids, 325 titration using β−galactosidase, 326– 328 transfection using Lipofectamine, 326–329 variations, 323, 324 genome, 321 replication, 321, 322 safety, 320 Simian immunodeficiency virus (SIV), gene transfer vectors, components, 353, 354 concentrating, 356, 358, 359 envelope protein selection, 354 Gag-Pol expression plasmid optimization, 355, 356 materials for production, 356 minimization of construct, 354, 355 plasmids, 356, 358 titration, 357–359 transfection, 356–359 genome structure, 351, 353 replication, 353 tropism and safety, 351 SIV, see Simian immunodeficiency virus Skin substitute, demand, 203 keratinocyte ex vivo retroviral gene transfer, acellular dermis preparation, 205, 206, 209, 210, 215 advantages of vector, 204 applications, 203, 204 cell culture, 204, 205, 208, 215

Index Skin substitute (cont.), keratinocyte ex vivo retroviral gene transfer (cont.), genetically modified skin substitute preparation, 206, 207, 210–212, 215 genetic modification of cells, 208, 209, 215 materials, 204–208, 214, 215 transplantation, 207, 212–214 Solvoplex, advantages of gene delivery, 83, 84 di-n-propylsulfoxide synthesis, 89, 90 formulations and efficiencies of lung gene transfer, 84, 85 intratracheal injection, mouse, 90–93 rat, 91 mechanism of transfection, 87 plasmid preparation, 88, 89 preparation, 90, 92 readministration, 87 reporter gene studies, β−galactosidase, 91–93 green fluorescent protein, 92, 93 luciferase, 91, 93 overview, 86 rodents for study, 88, 92 solvents, 88 storage, 86 toxicity, 87 T Titration, adeno-associated virus, herpes simplex virus-1 hybrid vectors, 468, 473, 474 recombinant vectors, 430, 431, 433, 438–442 adenovirus, helper-dependent vector system, 397, 406, 412 ovine vectors, 424, 425 feline immunodeficiency virus vectors, 347, 348, 347, 348 herpes simplex virus-1 vectors, 497

Index Titration (cont.), human immunodeficiency virus vectors, 266, 269, 270, 288, 290– 292.310, 313–315 retrovirus vectors, active virus per cell determination, 165, 169 cell culture, fibroblasts from human foreskin, 167, 168 materials, 166, 167 cell surface area determination by fluorescence microscopy, 167– 169 factors affecting titer, 161, 162 β−galactosidase assay, 167, 168, 171 multiplicity of infection determination, 165 recombinant retrovirus harvesting, 168 serial dilution, 161 start of infection, active virus concentration, 162–164, 169–172 transduction efficiency of different cell types, determination, 165, 166, 170, 171 Semliki forest virus vectors, 178, 184 Sendai virus vectors, 368 simian foamy virus-1 vectors, 326–328 simian immunodeficiency virus vectors, 357–359 vesicular stomatitis virus G glycoproteinpseudotyped murine leukemia retrovirus, 156 Transferrin receptor, gene delivery mediation, 33, 34 Tumor vaccine, antigens, 233 gene transfer, cytokine genes, allogeneic tumor vaccine clinical trials, 241, 242 animal studies, 237–239 autologous tumor vaccine clinical trials, 239, 240 mechanisms of antitumor immunity, 239

519 Tumor vaccine (cont.), gene transfer (cont.), cytokine genes (cont.), rationale, 235 selection of cytokine type, 237, 238 physical transfection methods, 235 retrovirus transduction, advantages and disadvantages, 235, 236 cytokine product assays, 244, 249– 251 gene transfer, 244, 247–249 materials, 242, 243 mouse challenge assay, 244, 245, 251, 252 producer cell maintenance, 243, 245 supernatant preparation, 243–246 tumor cell line maintenance, 244, 246, 247 viral vectors, 235, 236 T-cell antitumor immune response, 234, 235 V Vesicular stomatitis virus G glycoprotein (VSVG), asialoorosomucoid-lysine methyl esterVSVG peptide conjugate synthesis, 19, 20 feline immunodeficiency virus pseudotyping, 340, 341 human immunodeficiency virus pseudotyping, 261, 285, 306, 308, 319 murine leukemia retrovirus pseudotyping, cell culture, 153 concentrating, 156 env protein replacement, 150 materials, 153, 154 packaging cell, 150, 151 plasmids, 153 producer cell line generation, 155, 156 pseudotransduction, 152 rationale, 149, 150

520 Vesicular stomatitis virus G glycoprotein (VSVG) (cont.), murine leukemia retrovirus pseudotyping (cont.), titration, 156 transduction efficiency, 151, 152, 156, 157 transduction protocol, 154 transfection, 153–155, 157

Index Viral liposomes, see Hemagglutinating virus of Japan VSVG, see Vesicular stomatitis virus G glycoprotein W Woodchuck hepatitis virus, posttranscriptional regulatory element modification of HIV, 285

Gene Therapy Protocols

Gene Therapy Protocols

Gene Therapy